Compound and organic light-emitting device including the same

ABSTRACT

A compound is represented by Formula 1. An organic light-emitting device includes: a first electrode; a second electrode facing the first electrode; and an organic layer between the first electrode and the second electrode and including an emission layer, wherein the organic layer includes the compound represented by Formula 1. The compound represented by Formula 1 suppresses or reduces the generation of dark spots by chelating metal that migrates from an electrode.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims priority to and the benefit of Korean Patent Application No. 10-2019-0085206, filed on Jul. 15, 2019, in the Korean Intellectual Property Office, the entire content of which is incorporated herein by reference.

BACKGROUND 1. Field

One or more embodiments of the present disclosure relate to a compound and an organic light-emitting device including the same.

2. Description of the Related Art

Organic light-emitting devices (OLEDs) are self-emission devices that, as compared with other devices in the art, have wide viewing angles, high contrast ratios, short response times, and excellent characteristics in terms of brightness, driving voltage, and response speed, and produce full-color images.

The organic light-emitting device may include a first electrode on a substrate, and a hole transport region, an emission layer, an electron transport region, and a second electrode, which are sequentially on the first electrode. Holes provided from the first electrode may move toward the emission layer through the hole transport region, and electrons provided from the second electrode may move toward the emission layer through the electron transport region. Carriers, such as holes and electrons, recombine in the emission layer to produce excitons. Then, the excitons are transitioned (e.g., transition or relax) from an excited state to a ground state, thereby generating light.

SUMMARY

One or more embodiments of the present disclosure include a hole transport compound having high efficiency characteristics, as compared with an existing compound, and serving to suppress or reduce the generation of dark spots by chelating a metal that migrates from an electrode, and a device including the same.

Additional aspects of embodiments will be set forth in part in the description which follows and, in part, will be apparent from the description, or may be learned by practice of the presented embodiments.

An aspect of an embodiment of the present disclosure provides a compound represented by Formula 1:

In Formula 1,

-   -   A may be a single bond linked X₃ with X₄, or A may be a fused         C₄-C₆₀ carbocyclic group or a fused C₁-C₆₀ heterocyclic group,     -   X₁ may be N, C, or C(R₁₁), X₂ may be N, C, or C(R₁₂), X₃ may be         N, C, or C(R₁₃), X₄ may be N, C, or C(R₁₄), X₅ may be N, C, or         C(R₁₅), and X₆ may be N, C, or C(R₁₆),     -   Y₁ may be N or C(R₂₁), Y₂ may be N or C(R₂₂), Y₃ may be N or         C(R₂₃), and at least one of Y₁ to Y₃ may be N,     -   R₁ to R₄, R₁₁ to R₁₆, and R₂₁ to R₂₃ may each independently be         selected from hydrogen, deuterium, a substituted or         unsubstituted C₁-C₆₀ alkyl group, a substituted or unsubstituted         C₂-C₆₀ alkenyl group, a substituted or unsubstituted C₂-C₆₀         alkynyl group, a substituted or unsubstituted C₁-C₆₀ alkoxy         group, a substituted or unsubstituted C₃-C₁₀ cycloalkyl group, a         substituted or unsubstituted C₁-C₁₀ heterocycloalkyl group, a         substituted or unsubstituted C₃-C₁₀ cycloalkenyl group, a         substituted or unsubstituted C₁-C₁₀ heterocycloalkenyl group, a         substituted or unsubstituted C₆-C₆₀ aryl group, a substituted or         unsubstituted C₆-C₆₀ aryloxy group, a substituted or         unsubstituted C₆-C₆₀ arylthio group, a substituted or         unsubstituted C₁-C₆₀ heteroaryl group, a substituted or         unsubstituted monovalent non-aromatic condensed polycyclic         group, a substituted or unsubstituted monovalent non-aromatic         condensed heteropolycyclic group, —Si(Q₁)(Q₂)(Q₃), —N(Q₁)(Q₂),         —B(Q₁)(Q₂), —P(Q₁)(Q₂), —C(═O)(Q₁), —S(═O)₂(Q₁), and         —P(═O)(Q₁)(Q₂),     -   two neighboring substituents selected from R₁ to R₄, R₁₁ to R₁₆,         and R₂₁ to R₂₃ may be linked with each other to form a ring,     -   When A is a single bond linking X₃ with X₄, each of X₁, X₂, X₅,         and X₆ is CH, each of X₃ and X₄ is C, and R₁ may be excluded         from being hydrogen,     -   L may be selected from a substituted or unsubstituted C₄-C₆₀         carbocyclic group and a substituted or unsubstituted C₁-C₆₀         heterocyclic group,     -   When A is benzene, L or a moiety including Y₁ to Y₃ may be         linked with a carbon of position 3 (numerals 2 and 3 are carbon         positions where L; or the moiety including Y₁ to Y₃ (m=0) is         linked to the moiety including A),     -   m may be an integer from 0 to 3,     -   a may be 1 or 2,     -   b may be an integer from 1 to 4,     -   c and d may each independently be an integer from 1 to 5,

At least one substituent of the substituted C₁-C₆₀ alkyl group, the substituted C₂-C₆₀ alkenyl group, the substituted C₂-C₆₀ alkynyl group, the substituted C₁-C₆₀ alkoxy group, the substituted C₃-C₁₀ cycloalkyl group, the substituted C₁-C₁₀ heterocycloalkyl group, the substituted C₃-C₁₀ cycloalkenyl group, the substituted C₁—C₁₀ heterocycloalkenyl group, the substituted C₆-C₆₀ aryl group, the substituted C₆-C₆₀ arylene group, the substituted C₆-C₆₀ aryloxy group, the substituted C₆-C₆₀ arylthio group, the substituted C₁-C₆₀ heteroaryl group, the substituted C₁-C₆₀ heteroarylene group, the substituted monovalent non-aromatic condensed polycyclic group, the substituted monovalent non-aromatic condensed heteropolycyclic group, the substituted C₄-C₆₀ carbocyclic group, and the substituted C₁-C₆₀ heterocyclic group may be selected from:

-   -   deuterium (-D), —F, —Cl, —Br, —I, a hydroxyl group, a cyano         group, a nitro group, an amidino group, a hydrazino group, a         hydrazono group, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a         C₂-C₆₀ alkynyl group, and a C₁-C₆₀ alkoxy group;     -   a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl         group, and a C₁-C₆₀ alkoxy group, each substituted with at least         one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group,         a cyano group, a nitro group, an amidino group, a hydrazino         group, a hydrazono group, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀         heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀         heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy         group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a         monovalent non-aromatic condensed polycyclic group, a monovalent         non-aromatic condensed heteropolycyclic group,         —Si(Q₁₁)(Q₁₂)(Q₁₃), —N(Q₁₁)(Q₁₂), —B(Q₁₁)(Q₁₂), —C(═O)(Q₁₁),         —S(═O)₂(Q₁₁), and —P(═O)(Q₁₁)(Q₁₂);     -   a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a         C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a         C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio         group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic         condensed polycyclic group, and a monovalent non-aromatic         condensed heteropolycyclic group;     -   a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a         C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a         C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio         group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic         condensed polycyclic group, and a monovalent non-aromatic         condensed heteropolycyclic group, each substituted with at least         one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group,         a cyano group, a nitro group, an amidino group, a hydrazino         group, a hydrazono group, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl         group, a C₂-C₆₀ alkynyl group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀         cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀         cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀         aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a         C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed         polycyclic group, a monovalent non-aromatic condensed         heteropolycyclic group, —Si(Q₂₁)(Q₂₂)(Q₂₃), —N(Q₂₁)(Q₂₂),         —B(Q₂₁)(Q₂₂), —C(═O)(Q₂₁), —S(═O)₂(Q₂₁), and —P(═O)(Q₂₁)(Q₂₂);         and     -   —Si(Q₃₁)(Q₃₂)(Q₃₃), —N(Q₃₁)(Q₃₂), —B(Q₃₁)(Q₃₂), —C(═O)(Q₃₁),         —S(═O)₂(Q₃₁), and —P(═O)(Q₃₁)(Q₃₂), and     -   Q₁ to Q₃, Q₁₁ to Q₁₃, Q₂₁ to Q₂₃, and Q₃₁ to Q₃₃ may each         independently be selected from hydrogen, deuterium, —F, —Cl,         —Br, —I, a hydroxyl group, a cyano group, a nitro group, an         amidino group, a hydrazino group, a hydrazono group, a C₁-C₆₀         alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a         C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀         heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀         heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₁-C₆₀         heteroaryl group, a monovalent non-aromatic condensed polycyclic         group, a monovalent non-aromatic condensed heteropolycyclic         group, a biphenyl group, and a terphenyl group.

Another aspect of an embodiment of the present disclosure provides an organic light-emitting device including:

-   -   a first electrode;     -   a second electrode facing the first electrode; and     -   an organic layer between the first electrode and the second         electrode and including an emission layer,     -   wherein the organic layer includes the compound represented by         Formula 1.

Another aspect of an embodiment of the present disclosure provides an electronic apparatus including a thin-film transistor and the organic light-emitting device, wherein the thin-film transistor includes a source electrode, a drain electrode, an activation layer, and a gate electrode, and the first electrode of the organic light-emitting device is in electrical contact with one of the source electrode and the drain electrode of the thin-film transistor.

BRIEF DESCRIPTION OF THE DRAWINGS

These and/or other aspects of embodiments will become apparent and more readily appreciated from the following description of the embodiments, taken in conjunction with the accompanying drawings in which:

FIGS. 1 to 4 are schematic views of a structure of an organic light-emitting device according to an embodiment.

DETAILED DESCRIPTION

Reference will now be made in more detail to embodiments, examples of which are illustrated in the accompanying drawings, wherein like reference numerals refer to like elements throughout. In this regard, the present embodiments may have different forms and should not be construed as being limited to the descriptions set forth herein. Accordingly, the embodiments are merely described herein below, by referring to the figures, to explain aspects of embodiments of the present description. As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items. Expressions such as “at least one of,” when preceding a list of elements, modify the entire list of elements and do not modify the individual elements of the list.

External quantum efficiency (next) used in a light-emitting material layer may be obtained (or calculated) utilizing the following equation. η_(ext)=η_(int)×Γ×Φ×η_(out-coupling)

(wherein, η_(int): internal quantum efficiency, Γ: charge balance factor, Φ: radiative quantum efficiency, η_(out-coupling): out coupling efficiency).

Charge balance factor (r) refers to a balance of a hole and an electron forming an exciton and generally has a value of “1” on the assumption of 1:1 matching of 100%. Radiative quantum efficiency (Φ) is a value involved in luminescence efficiency of an actual light-emitting material and depends on fluorescence quantum efficiency of a dopant in a host-dopant system.

Internal quantum efficiency (ηint) refers to a ratio at which a generated exciton is converted into light that is emitted and has a limited value of up to 0.25 in the case of a fluorescent material. When a hole and an electron are recombined to form an exciton, singlet excitons and triplet excitons are generated at a ratio of 1:3 according to arrangements of electron spin. However, only the singlet excitons participate in light emission from the fluorescent material, and the remaining 75% of the triplet excitons do not participate in light emission from the fluorescent material.

Out coupling efficiency (η_(out-coupling)) refers to a ratio of light extracted to the outside from the emitted light. When isotropic molecules are thermally deposited to form a thin film, individual light-emitting molecules do not have a constant orientation (e.g., the same orientation) and exist in a random orientation state (e.g., the individual light-emitting molecules may be randomly oriented). Out coupling efficiency in such a random orientation state is generally assumed to be 0.2.

Therefore, in view of the above, maximum luminescence efficiency of an organic light-emitting diode device using a fluorescent material as the only light emitting material is about 5% or less. In order to overcome the low efficiency of the fluorescent material, a phosphorescent material has been developed which has a light-emitting mechanism that converts both singlet excitons and triplet excitons into light. In the case of red light and green light, a phosphorescent material having high luminescence efficiency has been developed, but in the case of blue light, a phosphorescent material having satisfactory luminescence efficiency and reliability has not been developed. Therefore, the development of a fluorescent material having satisfactory reliability and being capable of increasing luminescence efficiency by increasing quantum efficiency is desired.

An aspect of an embodiment of the present disclosure provides a compound represented by Formula 1:

In Formula 1,

-   -   A may be a single bond linking X₃ with X₄, or A may be a fused         C₄-C₆₀ carbocyclic group or a fused C₁-C₆₀ heterocyclic group,     -   X₁ may be N, C, or C(R₁₁), X₂ may be N, C, or C(R₁₂), X₃ may be         N, C, or C(R₁₃), X₄ may be N, C, or C(R₁₄), X₅ may be N, C, or         C(R₁₅), and X₆ may be N, C, or C(R₁₆),     -   Y₁ may be N or C(R₂₁), Y₂ may be N or C(R₂₂), Y₃ may be N or         C(R₂₃), and at least one selected from Y₁ to Y₃ may be N,     -   R₁ to R₄, R₁₁ to R₁₆, and R₂₁ to R₂₃ may each independently be         selected from hydrogen, deuterium, a substituted or         unsubstituted C₁-C₆₀ alkyl group, a substituted or unsubstituted         C₂-C₆₀ alkenyl group, a substituted or unsubstituted C₂-C₆₀         alkynyl group, a substituted or unsubstituted C₁-C₆₀ alkoxy         group, a substituted or unsubstituted C₃-C₁₀ cycloalkyl group, a         substituted or unsubstituted C₁-C₁₀ heterocycloalkyl group, a         substituted or unsubstituted C₃-C₁₀ cycloalkenyl group, a         substituted or unsubstituted C₁-C₁₀ heterocycloalkenyl group, a         substituted or unsubstituted C₆-C₆₀ aryl group, a substituted or         unsubstituted C₆-C₆₀ aryloxy group, a substituted or         unsubstituted C₆-C₆₀ arylthio group, a substituted or         unsubstituted C₁-C₆₀ heteroaryl group, a substituted or         unsubstituted monovalent non-aromatic condensed polycyclic         group, a substituted or unsubstituted monovalent non-aromatic         condensed heteropolycyclic group, —Si(Q₁)(Q₂)(Q₃), —N(Q₁)(Q₂),         —B(Q₁)(Q₂), —P(Q₁)(Q₂), —C(═O)(Q₁), —S(═O)₂(Q₁), and         —P(═O)(Q₁)(Q₂),     -   two neighboring substituents selected from R₁ to R₄, R₁₁ to R₁₆,         and R₂₁ to R₂₃ may be linked with each other to form a ring,     -   When A is a single bond linking X₃ with X₄, each of X₁, X₂, X₅,         and X₆ is CH, each of X₃ and X₄ is C, and R₁ may be excluded         from being hydrogen,     -   L may be selected from a substituted or unsubstituted C₄-C₆₀         carbocyclic group and a substituted or unsubstituted C₁-C₆₀         heterocyclic group,     -   When A is benzene, L or a moiety including Y₁ to Y₃ may be         linked with a carbon of position 3 (numerals 2 and 3 are carbon         positions where L; or the moiety including Y₁ to Y₃ (m=0) is         linked to the moiety including A),     -   m may be an integer from 0 to 3,     -   a may be 1 or 2,     -   b may be an integer from 1 to 4,     -   c and d may each independently be an integer from 1 to 5,     -   at least one substituent of the substituted C₁-C₆₀ alkyl group,         the substituted C₂-C₆₀ alkenyl group, the substituted C₂-C₆₀         alkynyl group, the substituted C₁-C₆₀ alkoxy group, the         substituted C₃-C₁₀ cycloalkyl group, the substituted C₁-C₁₀         heterocycloalkyl group, the substituted C₃-C₁₀ cycloalkenyl         group, the substituted C₁-C₁₀ heterocycloalkenyl group, the         substituted C₆-C₆₀ aryl group, the substituted C₆-C₆₀ arylene         group, the substituted C₆-C₆₀ aryloxy group, the substituted         C₆-C₆₀ arylthio group, the substituted C₁-C₆₀ heteroaryl group,         the substituted C₁-C₆₀ heteroarylene group, the substituted         monovalent non-aromatic condensed polycyclic group, the         substituted monovalent non-aromatic condensed heteropolycyclic         group, the substituted C₄-C₆₀ carbocyclic group, and the         substituted C₁-C₆₀ heterocyclic group may be selected from:     -   deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a         nitro group, an amidino group, a hydrazino group, a hydrazono         group, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀         alkynyl group, and a C₁-C₆₀ alkoxy group;     -   a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl         group, and a C₁-C₆₀ alkoxy group, each substituted with at least         one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group,         a cyano group, a nitro group, an amidino group, a hydrazino         group, a hydrazono group, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀         heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀         heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy         group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a         monovalent non-aromatic condensed polycyclic group, a monovalent         non-aromatic condensed heteropolycyclic group,         —Si(Q₁₁)(Q₁₂)(Q₁₃), —N(Q₁₁)(Q₁₂), —B(Q₁₁)(Q₁₂), —C(═O)(Q₁₁),         —S(═O)₂(Q₁₁), and —P(═O)(Q₁₁)(Q₁₂);     -   a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a         C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a         C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio         group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic         condensed polycyclic group, and a monovalent non-aromatic         condensed heteropolycyclic group;     -   a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a         C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a         C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio         group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic         condensed polycyclic group, and a monovalent non-aromatic         condensed heteropolycyclic group, each substituted with at least         one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group,         a cyano group, a nitro group, an amidino group, a hydrazino         group, a hydrazono group, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl         group, a C₂-C₆₀ alkynyl group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀         cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀         cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀         aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a         C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed         polycyclic group, a monovalent non-aromatic condensed         heteropolycyclic group, —Si(Q₂₁)(Q₂₂)(Q₂₃), —N(Q₂₁)(Q₂₂),         —B(Q₂₁)(Q₂₂), —C(═O)(Q₂₁), —S(═O)₂(Q₂₁) and —P(═O)(Q₂₁)(Q₂₂);         and     -   —Si(Q₃₁)(Q₃₂)(Q₃₃), —N(Q₃₁)(Q₃₂), —B(Q₃₁)(Q₃₂), —C(═O)(Q₃₁),         —S(═O)₂(Q₃₁), and —P(═O)(Q₃₁)(Q₃₂), and     -   Q₁ to Q₃, Q₁₁ to Q₁₃, Q₂₁ to Q₂₃, and Q₃₁ to Q₃₃ may each         independently be selected from hydrogen, deuterium, —F, —Cl,         —Br, —I, a hydroxyl group, a cyano group, a nitro group, an         amidino group, a hydrazino group, a hydrazono group, a C₁-C₆₀         alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a         C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀         heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀         heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₁-C₆₀         heteroaryl group, a monovalent non-aromatic condensed polycyclic         group, a monovalent non-aromatic condensed heteropolycyclic         group, a biphenyl group, and a terphenyl group.

For example, when A is benzene and b is 2 or more, neighboring R₂(s) may be linked with each other to form a ring.

In the compound represented by Formula 1 according to one or more embodiments, a stabilized form of a molecular structure has a flat molecular structure without rotation (e.g., in the flat molecular structure the pendant groups are not rotated out of the plane of the molecule). This molecular structure was confirmed based on a result of geometry optimization using density functional theory calculations performed utilizing Dmol3 software (available from Accelrys). The flat molecular structure of embodiments of the present disclosure provides a strong oscillator strength, which causes the molecules of the compound represented by Formula 1 to be aligned in the same (e.g., substantially the same) direction during deposition. The alignment of the molecules in the same (e.g., substantially the same) direction facilitates hole and electron movement, as compared with a random molecular structure (and/or a random orientation of the deposited material).

For example, as an example of the compound represented by Formula 1, when a compound having the following structure is geometry-optimized,

the following result may be obtained:

In some embodiments, the compound represented by Formula 1 includes two nitrogen atoms in

and thus, metal ion chelation by the compound represented by Formula 1 may be facilitated. Therefore, the diffusion into an emission layer is made impossible or unlikely by chelating metal ions migrating from an electrode. The generation of dark spots from metal ions that migrate from an electrode may be suppressed or reduced to prevent or reduce the occurrence of defective pixels of a panel.

In one embodiment, in Formula 1 X₁ to X₆ may each be C(R₁₁), C(R₁₂), C(R₁₃), C(R₁₄), C(R₁₅), C(R₁₆).

In one embodiment, in Formula 1 X₂ and X₅ may each be C(R₁₂) and C(R₁₅), and X₁ and X₆ may each be N.

In one embodiment, in Formula 1 X₂ and X₅ may each be N, and X₁ and X₆ may each be C(R₁₁) and C(R₁₆).

In one embodiment, A may be a single bond linking X₃ with X₄, a cyclopentane, a benzene, a naphthalene or a quinoxaline.

In one embodiment, in Formula 1 R₂ to R₄ may each be hydrogen or deuterium.

In one embodiment, in Formula 1 L may be a phenylene group, a naphthylene group, a phenanthrenylene group, an anthracenylene group, a pyrenylene group, a chrysenylene group, a pyridinylene group, a pyrazinylene group, a pyrimidinylene group, a pyridazinylene group, a quinolinylene group, an isoquinolinylene group, a quinoxalinylene group, a quinazolinylene group, a carbazolylene group, or a triazinylene group. When m is 2 or more, each L may be the same or different.

In one embodiment, Formula 1 may be one of the following Formula 1-1 to 1-7:

In Formulae 1-1 to 1-4 and 1-7, R′₂ and R″₂ may each independently be the same as defined in connection with R₂ in Formula 1. In Formula 1-5, R₁ may be excluded from being hydrogen. In Formulae 1-1 to 1-7, the substituents, subscripts, symbols, and the like may be the same as described with respect to Formula 1.

In one embodiment, R₁ in Formula 1 may be selected from hydrogen, deuterium, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a phenanthrenyl group, an anthracenyl group, a pyrenyl group, a chrysenyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, a quinolinyl group, an isoquinolinyl group, a quinoxalinyl group, a quinazolinyl group, a carbazolyl group, a benzofuropyridyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a triazinyl group, a benzimidazolyl group, and a phenanthrolinyl group.

In one embodiment, R₁ in Formula 1 may be hydrogen, deuterium, or a group represented by one of Formulae 2a and 2b:

In Formulae 2a and 2b, R₂₁ to R₂₃ may each independently be selected from hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazino group, a hydrazono group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₂₀ alkyl group, a C₁-C₂₀ alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a phenanthrenyl group, an anthracenyl group, a pyrenyl group, a chrysenyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, a quinolinyl group, an isoquinolinyl group, a quinoxalinyl group, a quinazolinyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a triazinyl group, a benzimidazolyl group, and a phenanthrolinyl group, a21 may be an integer from 1 to 4, a22 may be 1 or 2, a23 may be an integer from 1 to 3, and * indicates a binding site to a neighboring atom. When a21, a22, and a23 are each 2 or more, two or more R₂₁(s), two or more R₂₂(s), and two or more R₂₃(s) may be identical to or different from each other.

In one embodiment, the compound represented by Formula 1 may be one of the following compounds:

The expression “(an organic layer) includes at least one compound,” as used herein, may include a case in which “(an organic layer) includes identical compounds represented by Formula 1” and a case in which “(an organic layer) includes two or more different compounds represented by Formula 1”.

For example, the organic layer may include, as the compound represented by Formula 1, only Compound 1-1. In this regard, Compound 1-1 may exist only in the emission layer of the organic light-emitting device. In one or more embodiments, the organic layer may include, as the compound, Compound 1-1 and Compound 2-1. In this regard, Compound 1-1 and Compound 2-1 may exist in an identical layer (for example, Compound 1 and Compound 2 may all exist in an emission layer), or different layers (for example, Compound 1-1 may exist in an emission layer and Compound 2-1 may exist in an electron transport layer).

Another aspect of an embodiment of the present disclosure provides an organic light-emitting device including:

-   -   a first electrode;     -   a second electrode facing the first electrode; and     -   an organic layer between the first electrode and the second         electrode and including an emission layer,     -   wherein the organic layer includes the compound represented by         Formula 1.

In one embodiment,

-   -   the first electrode of the organic light-emitting device may be         an anode,     -   the second electrode of the organic light-emitting device may be         a cathode, and     -   the organic layer may further include a hole transport region         between the first electrode and the emission layer and an         electron transport region between the emission layer and the         second electrode,     -   the hole transport region may include a hole injection layer, a         hole transport layer, a buffer layer, an electron blocking         layer, or any combination thereof, and     -   the electron transport region may include a hole blocking layer,         an electron transport layer, an electron injection layer, or any         combination thereof.

In one embodiment, the emission layer may be a fluorescence emission layer.

In one embodiment, the compound represented by Formula 1 may be used in the hole transport region. For example, the compound represented by Formula 1 may be used in the hole transport layer.

Another aspect of an embodiment of the present disclosure provides an electronic apparatus including the organic light-emitting device and a thin-film transistor, wherein the first electrode of the organic light-emitting device may be in electrical contact with one of a source electrode and a drain electrode of the thin-film transistor.

The term “an organic layer,” as used herein, refers to a single layer and/or a plurality of layers between the first electrode and the second electrode of an organic light-emitting device. A material included in the “organic layer” is not limited to an organic material.

Description of FIG. 1

FIG. 1 is a schematic cross-sectional view of an organic light-emitting device 10 according to an embodiment. The organic light-emitting device 10 includes a first electrode 110, an organic layer 150, and a second electrode 190.

Hereinafter, the structure of an organic light-emitting device according to an embodiment and a method of manufacturing an organic light-emitting device according to an embodiment will be described in connection with FIG. 1 .

First Electrode 110

In FIG. 1 , a substrate may be additionally under the first electrode 110 or above the second electrode 190. For use as the substrate, the substrate may be a glass substrate or a plastic substrate, each having excellent mechanical strength, thermal stability, transparency, surface smoothness, ease of handling, and water resistance.

The first electrode 110 may be formed by depositing or sputtering a material for forming the first electrode 110 on the substrate. When the first electrode 110 is an anode, the material for forming the first electrode 110 may be selected from materials having a high work function to facilitate hole injection.

The first electrode 110 may be a reflective electrode, a semi-reflective electrode, or a transmissive electrode. When the first electrode 110 is a transmissive electrode, a material for forming a first electrode may be selected from indium tin oxide (ITO), indium zinc oxide (IZO), tin oxide (SnO₂), zinc oxide (ZnO), and any combinations thereof, but embodiments of the present disclosure are not limited thereto. In one or more embodiments, when the first electrode 110 is a semi-transmissive electrode or a reflectable electrode, a material for forming a first electrode may be selected from magnesium (Mg), silver (Ag), aluminum (Al), aluminum-lithium (Al—Li), calcium (Ca), magnesium-indium (Mg—In), magnesium-silver (Mg—Ag), and any combinations thereof, but embodiments of the present disclosure are not limited thereto.

The first electrode 110 may have a single-layered structure, or a multi-layered structure including two or more layers. For example, the first electrode 110 may have a three-layered structure of ITO/Ag/ITO, but the structure of the first electrode 110 is not limited thereto.

Organic Layer 150

The organic layer 150 is on the first electrode 110. The organic layer 150 may include an emission layer.

The organic layer 150 may further include a hole transport region between the first electrode 110 and the emission layer and an electron transport region between the emission layer and the second electrode 190.

Hole Transport Region in Organic Layer 150

The hole transport region may have i) a single-layered structure including a single layer including a single material, ii) a single-layered structure including a single layer including a plurality of different materials, or iii) a multi-layered structure having a plurality of layers including a plurality of different materials.

The hole transport region may include at least one layer selected from a hole injection layer, a hole transport layer, an emission auxiliary layer, and an electron blocking layer.

For example, the hole transport region may have a single-layered structure including a single layer including a plurality of different materials, or a multi-layered structure having a hole injection layer/hole transport layer structure, a hole injection layer/hole transport layer/emission auxiliary layer structure, a hole injection layer/emission auxiliary layer structure, a hole transport layer/emission auxiliary layer structure, or a hole injection layer/hole transport layer/electron blocking layer structure, wherein for each structure, constituting layers are sequentially stacked from the first electrode 110 in this stated order, but the structure of the hole transport region is not limited thereto.

The hole transport region may include at least one selected from m-MTDATA, TDATA, 2-TNATA, NPB(NPD), β-NPB, TPD, spiro-TPD, spiro-NPB, methylated-NPB, TAPC, HMTPD, 4,4′,4″-tris(N-carbazolyl)triphenylamine (TCTA), PANI/DBSA (polyaniline/dodecylbenzenesulfonic acid), poly(3,4-ethylenedioxythiophene)/poly(4-styrenesulfonate) (PEDOT/PSS), polyaniline/camphor sulfonic acid (PANI/CSA), and polyaniline/poly(4-styrenesulfonate) (PANI/PSS):

A thickness of the hole transport region may be from about 100 Å to about 10,000 Å, for example, about 100 Å to about 3,000 Å. When the hole transport region includes at least one selected from a hole injection layer and a hole transport layer, a thickness of the hole injection layer may be in a range of about 100 Å to about 9,000 Å, for example, about 100 Å to about 1,000 Å, and a thickness of the hole transport layer may be in a range of about 50 Å to about 2,000 Å, for example about 100 Å to about 1,500 Å. When the thicknesses of the hole transport region, the hole injection layer, and the hole transport layer are within these ranges, suitable or satisfactory hole transporting characteristics may be obtained without a substantial increase in driving voltage.

The emission auxiliary layer may increase light-emission efficiency by compensating for an optical resonance distance according to the wavelength of light emitted by an emission layer, and the electron blocking layer may block or reduce the flow of electrons from an electron transport region. The emission auxiliary layer and the electron blocking layer may include the materials as described herein above.

p-Dopant

The hole transport region may further include, in addition to these materials, a charge-generation material for the improvement of conductive (e.g., electrically conductive) properties. The charge-generation material may be homogeneously or non-homogeneously dispersed in the hole transport region.

The charge-generation material may be, for example, a p-dopant.

In one embodiment, the p-dopant may have a lowest unoccupied molecular orbital (LUMO) energy level of −3.5 eV or less.

The p-dopant may include at least one selected from a quinone derivative, a metal oxide, and a cyano group-containing compound, but embodiments of the present disclosure are not limited thereto.

In one embodiment, the p-dopant may include at least one selected from:

-   -   a quinone derivative, such as tetracyanoquinodimethane (TCNQ)         and 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane         (F4-TCNQ);     -   a metal oxide, such as tungsten oxide or molybdenum oxide;     -   1,4,5,8,9,12-hexaazatriphenylene-hexacarbonitrile (HAT-CN); and     -   a compound represented by Formula 221,     -   but embodiments of the present disclosure are not limited         thereto:

In Formula 221,

-   -   R₂₂₁ to R₂₂₃ may each independently be selected from a         substituted or unsubstituted C₃-C₁₀ cycloalkyl group, a         substituted or unsubstituted C₁-C₁₀ heterocycloalkyl group, a         substituted or unsubstituted C₃-C₁₀ cycloalkenyl group, a         substituted or unsubstituted C₁-C₁₀ heterocycloalkenyl group, a         substituted or unsubstituted C₆-C₆₀ aryl group, a substituted or         unsubstituted C₁-C₆₀ heteroaryl group, a substituted or         unsubstituted monovalent non-aromatic condensed polycyclic         group, and a substituted or unsubstituted monovalent         non-aromatic condensed heteropolycyclic group, wherein at least         one of R₂₂₁ to R₂₂₃ may have at least one substituent selected         from a cyano group, —F, —Cl, —Br, —I, a C₁-C₂₀ alkyl group         substituted with —F, a C₁-C₂₀ alkyl group substituted with —Cl,         a C₁-C₂₀ alkyl group substituted with —Br, and a C₁-C₂₀ alkyl         group substituted with —I.         Emission Layer in Organic Layer 150

When the organic light-emitting device 10 is a full-color organic light-emitting device, the emission layer may be patterned into a red emission layer, a green emission layer, and a blue emission layer. In one or more embodiments, the emission layer may have a stacked structure of two or more layers selected from a red emission layer, a green emission layer, and a blue emission layer, in which the two or more layers contact each other or are separated from each other. In one or more embodiments, the emission layer may include two or more materials selected from a red light-emitting material, a green light-emitting material, and a blue light-emitting material, in which the two or more materials are mixed with each other in a single layer to emit white light.

The emission layer may include a host and a dopant. The dopant may include at least one selected from a phosphorescent dopant and a fluorescent dopant.

In the emission layer, an amount of the dopant may be in a range of about 0.01 parts by weight to about 15 parts by weight based on 100 parts by weight of the host, but embodiments of the present disclosure are not limited thereto.

A thickness of the emission layer may be in a range of about 100 Å to about 1,000 Å, for example, about 200 Å to about 600 Å. When the thickness of the emission layer is within this range, excellent emission characteristics may be obtained without a substantial increase in driving voltage.

The emission layer may include a host.

Host in Emission Layer

In one or more embodiments, the host may further include a compound represented by Formula 2 below:

In Formula 2,

-   -   Ar₁ and Ar₂ may each independently be selected from a         substituted or unsubstituted C₆-C₆₀ aryl group and a substituted         or unsubstituted C₁-C₆₀ heteroaryl group,     -   R₁ to R₇ may each independently be selected from hydrogen,         deuterium, a substituted or unsubstituted C₁-C₆₀ alkyl group, a         substituted or unsubstituted C₆-C₆₀ aryl group, a substituted or         unsubstituted C₁-C₆₀ heteroaryl group, a substituted or         unsubstituted monovalent non-aromatic condensed polycyclic         group, and a substituted or unsubstituted monovalent         non-aromatic condensed heteropolycyclic group,     -   at least one substituent selected from the substituted C₁-C₆₀         alkyl group, the substituted C₆-C₆₀ aryl group, the substituted         C₁-C₆₀ heteroaryl group, the substituted monovalent non-aromatic         condensed polycyclic group, and the substituted monovalent         non-aromatic condensed heteropolycyclic group may be selected         from:     -   deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a         nitro group, an amidino group, a hydrazino group, a hydrazono         group, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀         alkynyl group, and a C₁-C₆₀ alkoxy group,     -   a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl         group, and a C₁-C₆₀ alkoxy group, each substituted with at least         one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group,         a cyano group, a nitro group, an amidino group, a hydrazino         group, a hydrazono group, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀         heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀         heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy         group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a         monovalent non-aromatic condensed polycyclic group, a monovalent         non-aromatic condensed heteropolycyclic group,         —Si(Q₁₁)(Q₁₂)(Q₁₃), —N(Q₁₁)(Q₁₂), —B(Q₁₁)(Q₁₂), —C(═O)(Q₁₁),         —S(═O)₂(Q₁₁), and —P(═O)(Q₁₁)(Q₁₂);     -   a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a         C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a         C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio         group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic         condensed polycyclic group, and a monovalent non-aromatic         condensed heteropolycyclic group;     -   a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a         C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a         C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio         group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic         condensed polycyclic group, and a monovalent non-aromatic         condensed heteropolycyclic group, each substituted with at least         one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group,         a cyano group, a nitro group, an amidino group, a hydrazino         group, a hydrazono group, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl         group, a C₂-C₆₀ alkynyl group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀         cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀         cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀         aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a         C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed         polycyclic group, a monovalent non-aromatic condensed         heteropolycyclic group, —Si(Q₂₁)(Q₂₂)(Q₂₃), —N(Q₂₁)(Q₂₂),         —B(Q₂₁)(Q₂₂), —C(═O)(Q₂₁), —S(═O)₂(Q₂₁), and —P(═O)(Q₂₁)(Q₂₂);         and     -   —Si(Q₃₁)(Q₃₂)(Q₃₃), —N(Q₃₁)(Q₃₂), —B(Q₃₁)(Q₃₂), —C(═O)(Q₃₁),         —S(═O)₂(Q₃₁), and —P(═O)(Q₃₁)(Q₃₂), and     -   Q₁ to Q₃, Q₁₁ to Q₁₃, Q₂₁ to Q₂₃, and Q₃₁ to Q₃₃ may each         independently be selected from hydrogen, deuterium, —F, —Cl,         —Br, —I, a hydroxyl group, a cyano group, a nitro group, an         amidino group, a hydrazino group, a hydrazono group, a C₁-C₆₀         alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a         C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀         heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀         heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₁-C₆₀         heteroaryl group, a monovalent non-aromatic condensed polycyclic         group, a monovalent non-aromatic condensed heteropolycyclic         group, a biphenyl group, and a terphenyl group.

The host may include at least one of the following compounds, but embodiments of the present disclosure are not limited thereto:

Phosphorescent Dopant Included in Emission Layer in Organic Layer 150

The phosphorescent dopant may include an organometallic complex represented by Formulae 401 or 402 below:

In Formulae 401 and 402,

-   -   M may be selected from iridium (Ir), platinum (Pt), palladium         (Pd), osmium (Os), titanium (Ti), zirconium (Zr), hafnium (Hf),         europium (Eu), terbium (Tb), rhodium (Rh), and thulium (Tm),     -   L₄₀₁ may be selected from ligands represented by Formula 402,         and xc1 may be 1, 2, or 3, wherein, when xc1 is 2 or more, two         or more L₄₀₁(s) may be identical to or different from each         other,     -   L₄₀₂ may be an organic ligand, and xc2 may be an integer from 0         to 4, wherein, when xc2 is two or more, two or more L₄₀₂(s) may         be identical to or different from each other,     -   X₄₀₁ to X₄₀₄ may each independently be nitrogen or carbon,     -   X₄₀₁ and X₄₀₃ may be linked via a single bond or a double bond,         and X₄₀₂ and X₄₀₄ may be linked via a single bond or a double         bond,     -   A₄₀₁ and A₄₀₂ may each independently be selected from a C₅-C₆₀         carbocyclic group or a C₁-C₆₀ heterocyclic group,     -   X₄₀₅ may be a single bond, *—O—*′, *—S—*′, *—C(═O)—*′,         *—N(Q₄₁₁)—*′, *—C(Q₄₁₁)(Q₄₁₂)—*′, *—C(Q₄₁₁)═C(Q₄₁₂)—*,         *—C(Q₄₁₁)=*′, or *═C(Q₄₁₁)=*′, wherein Q₄₁₁ and Q₄₁₂ may each         independently be hydrogen, deuterium, a C₁-C₂₀ alkyl group, a         C₁-C₂₀ alkoxy group, a phenyl group, a biphenyl group, a         terphenyl group, or a naphthyl group,     -   X₄₀₆ may be a single bond, O, or S,     -   R₄₀₁ and R₄₀₂ may each independently be selected from hydrogen,         deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a         nitro group, an amidino group, a hydrazino group, a hydrazono         group, a substituted or unsubstituted C₁-C₂₀ alkyl group, a         substituted or unsubstituted C₁-C₂₀ alkoxy group, a substituted         or unsubstituted C₃-C₁₀ cycloalkyl group, a substituted or         unsubstituted C₁-C₁₀ heterocycloalkyl group, a substituted or         unsubstituted C₃-C₁₀ cycloalkenyl group, a substituted or         unsubstituted C₁-C₁₀ heterocycloalkenyl group, a substituted or         unsubstituted C₆-C₆₀ aryl group, a substituted or unsubstituted         C₆-C₆₀ aryloxy group, a substituted or unsubstituted C₆-C₆₀         arylthio group, a substituted or unsubstituted C₁-C₆₀ heteroaryl         group, a substituted or unsubstituted monovalent non-aromatic         condensed polycyclic group, and a substituted or unsubstituted         monovalent non-aromatic condensed heteropolycyclic group,         —Si(Q₄₀₁)(Q₄₀₂)(Q₄₀₃), —N(Q₄₀₁)(Q₄₀₂), —B(Q₄₀₁)(Q₄₀₂),         —C(═O)(Q₄₀₁), —S(═O)₂(Q₄₀₁), and —P(═O)(Q₄₀₁)(Q₄₀₂), wherein         Q₄₀₁ to Q₄₀₃ may each independently be selected from a C₁-C₁₀         alkyl group, a C₁-C₁₀ alkoxy group, a C₆-C₂₀ aryl group, and a         C₁-C₂₀ heteroaryl group,     -   xc11 and xc12 may each independently be an integer from 0 to 10,         and     -   * and *′ in Formula 402 each indicate a binding site to M in         Formula 401.

In one embodiment, A₄₀₁ and A₄₀₂ in Formula 402 may each independently be selected from a benzene group, a naphthalene group, a fluorene group, a spiro-bifluorene group, an indene group, a pyrrole group, a thiophene group, a furan group, an imidazole group, a pyrazole group, a thiazole group, an isothiazole group, an oxazole group, an isoxazole group, a pyridine group, a pyrazine group, a pyrimidine group, a pyridazine group, a quinoline group, an isoquinoline group, a benzoquinoline group, a quinoxaline group, a quinazoline group, a carbazole group, a benzimidazole group, a benzofuran group, a benzothiophene group, an isobenzothiophene group, a benzoxazole group, an isobenzoxazole group, a triazole group, a tetrazole group, an oxadiazole group, a triazine group, a dibenzofuran group, and a dibenzothiophene group.

In one or more embodiments, in Formula 402, i) X₄₀₁ may be nitrogen, and X₄₀₂ may be carbon, or ii) X₄₀₁ and X₄₀₂ may each be nitrogen at the same time.

In one or more embodiments, R₄₀₁ and R₄₀₂ in Formula 402 may each independently be selected from:

-   -   hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano         group, a nitro group, an amidino group, a hydrazino group, a         hydrazono group, a C₁-C₂₀ alkyl group, and a C₁-C₂₀ alkoxy         group;     -   a C₁-C₂₀ alkyl group and a C₁-C₂₀ alkoxy group, each substituted         with at least one selected from deuterium, —F, —Cl, —Br, —I, a         hydroxyl group, a cyano group, a nitro group, an amidino group,         a hydrazino group, a hydrazono group, a phenyl group, a naphthyl         group, a cyclopentyl group, a cyclohexyl group, an adamantanyl         group, a norbornanyl group, and a norbornenyl group;     -   a cyclopentyl group, a cyclohexyl group, an adamantanyl group, a         norbornanyl group, a norbornenyl group, a phenyl group, a         biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl         group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl         group, a pyridazinyl group, a triazinyl group, a quinolinyl         group, an isoquinolinyl group, a quinoxalinyl group, a         quinazolinyl group, a carbazolyl group, a dibenzofuranyl group,         and a dibenzothiophenyl group;     -   a cyclopentyl group, a cyclohexyl group, an adamantanyl group, a         norbornanyl group, a norbornenyl group a phenyl group, a         biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl         group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl         group, a pyridazinyl group, a triazinyl group, a quinolinyl         group, an isoquinolinyl group, a quinoxalinyl group, a         quinazolinyl group, a carbazolyl group, a dibenzofuranyl group,         and a dibenzothiophenyl group, each substituted with at least         one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group,         a cyano group, a nitro group, an amidino group, a hydrazino         group, a hydrazono group, a C₁-C₂₀ alkyl group, a C₁-C₂₀ alkoxy         group, a cyclopentyl group, a cyclohexyl group, an adamantanyl         group, a norbornanyl group, a norbornenyl group, a phenyl group,         a biphenyl group, a terphenyl group, a naphthyl group, a         fluorenyl group, a pyridinyl group, a pyrazinyl group, a         pyrimidinyl group, a pyridazinyl group, a triazinyl group, a         quinolinyl group, an isoquinolinyl group, a quinoxalinyl group,         a quinazolinyl group, a carbazolyl group, a dibenzofuranyl         group, and a dibenzothiophenyl group; and     -   —Si(Q₄₀₁)(Q₄₀₂)(Q₄₀₃), —N(Q₄₀₁)(Q₄₀₂), —B(Q₄₀₁)(Q₄₀₂),         —C(═O)(Q₄₀₁), —S(═O)₂(Q₄₀₁) and —P(═O)(Q₄₀₁)(Q₄₀₂),     -   Q₄₀₁ to Q₄₀₃ may each independently be selected from a C₁-C₁₀         alkyl group, a C₁-C₁₀ alkoxy group, a phenyl group, a biphenyl         group, and a naphthyl group, but embodiments of the present         disclosure are not limited thereto.

In one or more embodiments, when xc1 in Formula 401 is 2 or more, two A₄₀₁(s) in two or more L₄₀₁(s) may optionally be linked via X₄₀₇, which is a linking group, or two A₄₀₂(s) in two or more L₄₀₁(s) may optionally be linked via X₄₀₈, which is a linking group (see Compounds PD1 to PD4 and PD7). X₄₀₇ and X₄₀₈ may each independently be a single bond, *—O—*′, *—S—*′, *—C(═O)—*′, *—N(Q₄₁₃)—*′, *—C(Q₄₁₃)(Q₄₁₄)—*′, or *—C(Q₄₁₃)═C(Q₄₁₄)—*′(wherein Q₄₁₃ and Q₄₁₄ may each independently be hydrogen, deuterium, a C₁-C₂₀ alkyl group, a C₁-C₂₀ alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, or a naphthyl group), but embodiments of the present disclosure are not limited thereto.

L₄₀₂ in Formula 401 may be a monovalent, divalent, or trivalent organic ligand. For example, L₄₀₂ may be selected from halogen, diketone (for example, acetylacetonate), carboxylic acid (for example, picolinate), —C(═O), isonitrile, —CN, and phosphorus (for example, phosphine, or phosphite), but embodiments of the present disclosure are not limited thereto.

In one or more embodiments, the phosphorescent dopant may be selected from, for example, Compounds PD1 to PD25, but embodiments of the present disclosure are not limited thereto:

Fluorescent Dopant in Emission Layer

The fluorescent dopant may include an arylamine compound or a styrylamine compound.

The fluorescent dopant may include a compound represented by Formula 501 below:

In Formula 501,

-   -   Ar₅₀₁ may be a substituted or unsubstituted C₄-C₆₀ carbocyclic         group or a substituted or unsubstituted C₁-C₆₀ heterocyclic         group,     -   L₅₀₁ to L₅₀₃ may each independently be selected from a         substituted or unsubstituted C₃-C₁₀ cycloalkylene group, a         substituted or unsubstituted C₁-C₁₀ heterocycloalkylene group, a         substituted or unsubstituted C₃-C₁₀ cycloalkenylene group, a         substituted or unsubstituted C₁-C₁₀ heterocycloalkenylene group,         a substituted or unsubstituted C₆-C₆₀ arylene group, a         substituted or unsubstituted C₁-C₆₀ heteroarylene group, a         substituted or unsubstituted divalent non-aromatic condensed         polycyclic group, and a substituted or unsubstituted divalent         non-aromatic condensed heteropolycyclic group,     -   xd1 to xd3 may each independently be an integer from 0 to 3,     -   R₅₀₁ and R₅₀₂ may each independently be selected from a         substituted or unsubstituted C₃-C₁₀ cycloalkyl group, a         substituted or unsubstituted C₁-C₁₀ heterocycloalkyl group, a         substituted or unsubstituted C₃-C₁₀ cycloalkenyl group, a         substituted or unsubstituted C₁-C₁₀ heterocycloalkenyl group, a         substituted or unsubstituted C₆-C₆₀ aryl group, a substituted or         unsubstituted C₆-C₆₀ aryloxy group, a substituted or         unsubstituted C₆-C₆₀ arylthio group, a substituted or         unsubstituted C₁-C₆₀ heteroaryl group, a substituted or         unsubstituted monovalent non-aromatic condensed polycyclic         group, and a substituted or unsubstituted monovalent         non-aromatic condensed heteropolycyclic group, and     -   xd4 may be an integer from 1 to 6.

In one embodiment, in Formula 501, Ar₅₀₁ may be selected from:

-   -   a naphthalene group, a heptalene group, a fluorene group, a         spiro-bifluorene group, a benzofluorene group, a dibenzofluorene         group, a phenalene group, a phenanthrene group, an anthracene         group, a fluoranthene group, a triphenylene group, a pyrene         group, a chrysene group, a naphthacene group, a picene group, a         perylene group, a pentaphene group, an indenoanthracene group,         and an indenophenanthrene group; and     -   a naphthalene group, a heptalene group, a fluorene group, a         spiro-bifluorene group, a benzofluorene group, a dibenzofluorene         group, a phenalene group, a phenanthrene group, an anthracene         group, a fluoranthene group, a triphenylene group, a pyrene         group, a chrysene group, a naphthacene group, a picene group, a         perylene group, a pentaphene group, an indenoanthracene group,         and an indenophenanthrene group, each substituted with at least         one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group,         a cyano group, a nitro group, an amidino group, a hydrazino         group, a hydrazono group, a C₁-C₂₀ alkyl group, a C₁-C₂₀ alkoxy         group, a phenyl group, a biphenyl group, a terphenyl group, and         a naphthyl group.

In one or more embodiments, L₅₀₁ to L₅₀₃ in Formula 501 may each independently be selected from:

-   -   a phenylene group, a naphthylene group, a fluorenylene group, a         spiro-bifluorenylene group, a benzofluorenylene group, a         dibenzofluorenylene group, a phenanthrenylene group, an         anthracenylene group, a fluoranthenylene group, a         triphenylenylene group, a pyrenylene group, a chrysenylene         group, a perylenylene group, a pentaphenylene group, a         hexacenylene group, a pentacenylene group, a thiophenylene         group, a furanylene group, a carbazolylene group, an indolylene         group, an isoindolylene group, a benzofuranylene group, a         benzothiophenylene group, a dibenzofuranylene group, a         dibenzothiophenylene group, a benzocarbazolylene group, a         dibenzocarbazolylene group, a dibenzosilolylene group, and a         pyridinylene group; and     -   a phenylene group, a naphthylene group, a fluorenylene group, a         spiro-bifluorenylene group, a benzofluorenylene group, a         dibenzofluorenylene group, a phenanthrenylene group, an         anthracenylene group, a fluoranthenylene group, a         triphenylenylene group, a pyrenylene group, a chrysenylene         group, a perylenylene group, a pentaphenylene group, a         hexacenylene group, a pentacenylene group, a thiophenylene         group, a furanylene group, a carbazolylene group, an indolylene         group, an isoindolylene group, a benzofuranylene group, a         benzothiophenylene group, a dibenzofuranylene group, a         dibenzothiophenylene group, a benzocarbazolylene group, a         dibenzocarbazolylene group, a dibenzosilolylene group, and a         pyridinylene group, each substituted with at least one selected         from deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano         group, a nitro group, an amidino group, a hydrazino group, a         hydrazono group, a C₁-C₂₀ alkyl group, a C₁-C₂₀ alkoxy group, a         phenyl group, a biphenyl group, a terphenyl group, a naphthyl         group, a fluorenyl group, a spiro-bifluorenyl group, a         benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl         group, an anthracenyl group, a fluoranthenyl group, a         triphenylenyl group, a pyrenyl group, a chrysenyl group, a         perylenyl group, a pentaphenyl group, a hexacenyl group, a         pentacenyl group, a thiophenyl group, a furanyl group, a         carbazolyl group, an indolyl group, an isoindolyl group, a         benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl         group, a dibenzothiophenyl group, a benzocarbazolyl group, a         dibenzocarbazolyl group, a dibenzosilolyl group, and a pyridinyl         group.

In one or more embodiments, R₅₀₁ and R₅₀₂ in Formula 501 may each independently be selected from:

-   -   a phenyl group, a biphenyl group, a terphenyl group, a naphthyl         group, a fluorenyl group, a spiro-bifluorenyl group, a         benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl         group, an anthracenyl group, a fluoranthenyl group, a         triphenylenyl group, a pyrenyl group, a chrysenyl group, a         perylenyl group, a pentaphenyl group, a hexacenyl group, a         pentacenyl group, a thiophenyl group, a furanyl group, a         carbazolyl group, an indolyl group, an isoindolyl group, a         benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl         group, a dibenzothiophenyl group, a benzocarbazolyl group, a         dibenzocarbazolyl group, a dibenzosilolyl group, and a pyridinyl         group; and     -   a phenyl group, a biphenyl group, a terphenyl group, a naphthyl         group, a fluorenyl group, a spiro-bifluorenyl group, a         benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl         group, an anthracenyl group, a fluoranthenyl group, a         triphenylenyl group, a pyrenyl group, a chrysenyl group, a         perylenyl group, a pentaphenyl group, a hexacenyl group, a         pentacenyl group, a thiophenyl group, a furanyl group, a         carbazolyl group, an indolyl group, an isoindolyl group, a         benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl         group, a dibenzothiophenyl group, a benzocarbazolyl group, a         dibenzocarbazolyl group, a dibenzosilolyl group, and a pyridinyl         group, each substituted with at least one selected from         deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a         nitro group, an amidino group, a hydrazino group, a hydrazono         group, a C₁-C₂₀ alkyl group, a C₁-C₂₀ alkoxy group, a phenyl         group, a biphenyl group, a terphenyl group, a naphthyl group, a         fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl         group, a dibenzofluorenyl group, a phenanthrenyl group, an         anthracenyl group, a fluoranthenyl group, a triphenylenyl group,         a pyrenyl group, a chrysenyl group, a perylenyl group, a         pentaphenyl group, a hexacenyl group, a pentacenyl group, a         thiophenyl group, a furanyl group, a carbazolyl group, an         indolyl group, an isoindolyl group, a benzofuranyl group, a         benzothiophenyl group, a dibenzofuranyl group, a         dibenzothiophenyl group, a benzocarbazolyl group, a         dibenzocarbazolyl group, a dibenzosilolyl group, a pyridinyl         group, and —Si(Q₃₁)(Q₃₂)(Q₃₃), and     -   Q₃₁ to Q₃₃ may each independently be selected from a C₁-C₁₀         alkyl group, a C₁-C₁₀ alkoxy group, a phenyl group, a biphenyl         group, a terphenyl group, and a naphthyl group.

In one or more embodiments, xd4 in Formula 501 may be 2, but embodiments of the present disclosure are not limited thereto.

For example, the fluorescent dopant may be selected from Compounds FD1 to FD22:

In one or more embodiments, the fluorescent dopant may be selected from the following compounds, but embodiments of the present disclosure are not limited thereto:

Quantum Dot in Emission Layer

In one embodiment, the emission layer included in the organic light-emitting device may include a quantum dot material.

The quantum dot is a particle having a crystal structure having a size of several to tens of nanometers and may include hundreds to thousands of atoms.

Because the quantum dot is very small in size, the quantum dot may exhibit a quantum confinement effect. The quantum confinement effect refers to a phenomenon in which a band gap of an object increases when the object becomes smaller than a nanometer size. Therefore, when light of a wavelength having an energy greater than the band gap of the quantum dot is irradiated onto the quantum dot, the quantum dot absorbs the light and is promoted to an excited state, and emits light of a set or specific wavelength when it returns to a ground state. At this time, the wavelength of the emitted light has a value corresponding to the band gap.

A core of the quantum dot may include a group II-VI compound, a group III-VI compound, a group III-V compound, a group IV-VI compound, a group IV compound, a group I-III-VI compound, or any mixture thereof.

The group IV-VI compound may be selected from: a binary compound selected from SnS, SnSe, SnTe, PbS, PbSe, PbTe, and any mixture thereof; a ternary compound selected from SnSeS, SnSeTe, SnSTe, PbSeS, PbSeTe, PbSTe, SnPbS, SnPbSe, SnPbTe, and any mixture thereof; and a quaternary compound selected from SnPbSSe, SnPbSeTe, SnPbSTe, and any mixture thereof. The group IV element may be selected from Si, Ge, and any mixture thereof. The group IV compound may be a binary compound selected from SiC, SiGe, and any mixture thereof.

The binary compound, the ternary compound, or the quaternary compound may exist in particles at uniform (e.g., substantially uniform) concentration, or may exist in the same particle in a state in which a concentration distribution is partially different. In addition, the binary compound, the ternary compound, or the quaternary compound may have a core-shell structure in which one quantum dot surrounds another quantum dot. An interface between the core and the shell may have a concentration gradient in which the concentration of certain atoms existing in the shell decreases along a direction toward the center.

In one or more embodiments, the quantum dot may have a core-shell structure including a core with the above-described nanoparticles and a shell surrounding the core. The shell of the quantum dot may serve as a protective layer for maintaining semiconductor characteristics by preventing or reducing chemical degeneration of the core and/or may serve as a charging layer for imparting electrophoretic characteristics to the quantum dot. The shell may be a single layer or a multilayer. An interface between the core and the shell may have a concentration gradient in which the concentration of certain atoms existing in the shell decreases along a direction toward the center. Examples of the shell of the quantum dot may include a metal or non-metal oxide, a semiconductor compound, or any combination thereof.

For example, examples of the metal or non-metal oxide may include a binary compound such as SiO₂, Al₂O₃, TiO₂, ZnO, MnO, Mn₂O₃, Mn₃O₄, CuO, FeO, Fe₂O₃, Fe₃O₄, CoO, Co₃O₄, NiO, or a ternary compound such as MgAl₂O₄, CoFe₂O₄, NiFe₂O₄, or CoMn₂O₄, but embodiments of the present disclosure are not limited thereto.

In addition, examples of the semiconductor compound may include CdS, CdSe, CdTe, ZnS, ZnSe, ZnTe, ZnSeS, ZnTeS, GaAs, GaP, GaSb, HgS, HgSe, HgTe, InAs, InP, InGaP, InSb, AlAs, AlP, AlSb, and the like, but embodiments of the present disclosure are not limited thereto.

A full width of half maximum (FWHM) of an emission wavelength spectrum of the quantum dot may be about 45 nm or less, for example, about 40 nm or less, for example, about 30 nm or less. When the FWHM of the emission wavelength spectrum of the quantum dot is within this range, color purity or color reproduction may be improved. In addition, light emitted through such quantum dot is irradiated in omnidirection (e.g., substantially every direction), thereby improving a wide viewing angle.

In addition, the quantum dot is a quantum dot generally used in the art, and is not particularly limited. For example, a spherical, pyramidal, multi-arm, or cubic nanoparticle, nanotube, nanowire, nanofiber, or nanoplate particle may be used.

The quantum dot may adjust the color of emitted light according to the particle size. Therefore, the quantum dot may be configured to emit various suitable emission colors such as blue, red, or green.

Electron Transport Region in Organic Layer 150

The electron transport region may have i) a single-layered structure including a single layer including a single material, ii) a single-layered structure including a single layer including a plurality of different materials, or iii) a multi-layered structure having a plurality of layers including a plurality of different materials.

The electron transport region may include at least one selected from a hole blocking layer, an electron control layer, an electron transport layer, and an electron injection layer, but embodiments of the present disclosure are not limited thereto.

For example, the electron transport region may have an electron transport layer/electron injection layer structure, a hole blocking layer/electron transport layer/electron injection layer structure, an electron control layer/electron transport layer/electron injection layer structure, or an electron transport layer/electron injection layer structure, wherein for each structure, constituting layers are sequentially stacked from an emission layer. However, embodiments of the structure of the electron transport region are not limited thereto.

The electron transport region may include the organic layer including the compound represented by Formula 1.

The electron transport region may further include, in addition to the compound represented by Formula 1, for example, a compound represented by Formula 601: [Ar₆₀₁]_(xe11)-[(L₆₀₁)_(xe11)-R₆₀₁]_(xe21).  Formula 601

In Formula 601,

-   -   Ar₆₀₁ may be a substituted or unsubstituted C₄-C₆₀ carbocyclic         group or a substituted or unsubstituted C₁-C₆₀ heterocyclic         group,     -   xe11 may be 1, 2, or 3,     -   L₆₀₁ may be selected from a substituted or unsubstituted C₃-C₁₀         cycloalkylene group, a substituted or unsubstituted C₁-C₁₀         heterocycloalkylene group, a substituted or unsubstituted C₃-C₁₀         cycloalkenylene group, a substituted or unsubstituted C₁-C₁₀         heterocycloalkenylene group, a substituted or unsubstituted         C₆-C₆₀ arylene group, a substituted or unsubstituted C₁-C₆₀         heteroarylene group, a substituted or unsubstituted divalent         non-aromatic condensed polycyclic group, and a substituted or         unsubstituted divalent non-aromatic condensed heteropolycyclic         group,     -   xe1 may be an integer from 0 to 5,     -   R₆₀₁ may be selected from a substituted or unsubstituted C₃-C₁₀         cycloalkyl group, a substituted or unsubstituted C₁-C₁₀         heterocycloalkyl group, a substituted or unsubstituted C₃-C₁₀         cycloalkenyl group, a substituted or unsubstituted C₁-C₁₀         heterocycloalkenyl group, a substituted or unsubstituted C₆-C₆₀         aryl group, a substituted or unsubstituted C₆-C₆₀ aryloxy group,         a substituted or unsubstituted C₆-C₆₀ arylthio group, a         substituted or unsubstituted C₁-C₆₀ heteroaryl group, a         substituted or unsubstituted monovalent non-aromatic condensed         polycyclic group, a substituted or unsubstituted monovalent         non-aromatic condensed heteropolycyclic group,         —Si(Q₆₀₁)(Q₆₀₂)(Q₆₃), —C(═O)(Q₆₀₁), —S(═O)₂(Q₆₀₁), and         —P(═O)(Q₆₀₁)(Q₆₀₂),     -   Q₆₀₁ to Q₆₀₃ may each independently be a C₁-C₁₀ alkyl group, a         C₁-C₁₀ alkoxy group, a phenyl group, a biphenyl group, a         terphenyl group, or a naphthyl group, and     -   xe21 may be an integer from 1 to 5.

In one embodiment, at least one of Ar₆₀₁(s) in the number of xe11 and R₆₁(s) in the number of xe21 may include the π electron-depleted nitrogen-containing ring.

In one embodiment, Ar₆₀₁ in Formula 601 may be selected from:

-   -   a benzene group, a naphthalene group, a fluorene group, a         spiro-bifluorene group, a benzofluorene group, a dibenzofluorene         group, a phenalene group, a phenanthrene group, an anthracene         group, a fluoranthene group, a triphenylene group, a pyrene         group, a chrysene group, a naphthacene group, a picene group, a         perylene group, a pentaphene group, an indenoanthracene group, a         dibenzofuran group, a dibenzothiophene group, a carbazole group,         an imidazole group, a pyrazole group, a thiazole group, an         isothiazole group, an oxazole group, an isoxazole group, a         pyridine group, a pyrazine group, a pyrimidine group, a         pyridazine group, an indazole group, a purine group, a quinoline         group, an isoquinoline group, a benzoquinoline group, a         phthalazine group, a naphthyridine group, a quinoxaline group, a         quinazoline group, a cinnoline group, a phenanthridine group, an         acridine group, a phenanthroline group, a phenazine group, a         benzimidazole group, an isobenzothiazole group, a benzoxazole         group, an isobenzoxazole group, a triazole group, a tetrazole         group, an oxadiazole group, a triazine group, a thiadiazole         group, an imidazopyridine group, an imidazopyrimidine group, and         an azacarbazole group; and     -   a benzene group, a naphthalene group, a fluorene group, a         spiro-bifluorene group, a benzofluorene group, a dibenzofluorene         group, a phenalene group, a phenanthrene group, an anthracene         group, a fluoranthene group, a triphenylene group, a pyrene         group, a chrysene group, a naphthacene group, a picene group, a         perylene group, a pentaphene group, an indenoanthracene group, a         dibenzofuran group, a dibenzothiophene group, a carbazole group,         an imidazole group, a pyrazole group, a thiazole group, an         isothiazole group, an oxazole group, an isoxazole group, a         pyridine group, a pyrazine group, a pyrimidine group, a         pyridazine group, an indazole group, a purine group, a quinoline         group, an isoquinoline group, a benzoquinoline group, a         phthalazine group, a naphthyridine group, a quinoxaline group, a         quinazoline group, a cinnoline group, a phenanthridine group, an         acridine group, a phenanthroline group, a phenazine group, a         benzimidazole group, an isobenzothiazole group, a benzoxazole         group, an isobenzoxazole group, a triazole group, a tetrazole         group, an oxadiazole group, a triazine group, a thiadiazole         group, an imidazopyridine group, an imidazopyrimidine group, and         an azacarbazole group, each substituted with at least one         selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a         cyano group, a nitro group, an amidino group, a hydrazino group,         a hydrazono group, a C₁-C₂₀ alkyl group, a C₁-C₂₀ alkoxy group,         a phenyl group, a biphenyl group, a terphenyl group, a naphthyl         group, —Si(Q₃₁)(Q₃₂)(Q₃₃), —S(═O)₂(Q₃₁), and —P(═O)(Q₃₁)(Q₃₂),         and     -   Q₃₁ to Q₃₃ may each independently be selected from a C₁-C₁₀         alkyl group, a C₁-C₁₀ alkoxy group, a phenyl group, a biphenyl         group, a terphenyl group, and a naphthyl group.

When xe11 in Formula 601 is 2 or more, two or more Ar₆₀₁(s) may be linked via a single bond.

In one or more embodiments, Ar₆₀₁ in Formula 601 may be an anthracene group.

In one or more embodiments, a compound represented by Formula 601 may be represented by Formula 601-1 below:

In Formula 601-1,

-   -   X₆₁₄ may be N or C(R₆₁₄), X₆₁₅ may be N or C(R₆₁₅), X₆₁₆ may be         N or C(R₆₁₆), and at least one selected from X₆₁₄ to X₆₁₆ may be         N,

L₆₁₁ to L₆₁₃ may each independently be the same as described in connection with L₆₀₁,

-   -   xe611 to xe613 may each independently be defined the same as         xe1,     -   R₆₁₁ to R₆₁₃ may each independently be the same as described in         connection with R₆₀₁, and     -   R₆₁₄ to R₆₁₆ may each independently be selected from hydrogen,         deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a         nitro group, an amidino group, a hydrazino group, a hydrazono         group, a C₁-C₂₀ alkyl group, a C₁-C₂₀ alkoxy group, a phenyl         group, a biphenyl group, a terphenyl group, and a naphthyl         group.

In one embodiment, L₆₀₁ and L₆₁₁ to L₆₁₃ in Formulae 601 and 601-1 may each independently be selected from:

-   -   a phenylene group, a naphthylene group, a fluorenylene group, a         spiro-bifluorenylene group, a benzofluorenylene group, a         dibenzofluorenylene group, a phenanthrenylene group, an         anthracenylene group, a fluoranthenylene group, a         triphenylenylene group, a pyrenylene group, a chrysenylene         group, a perylenylene group, a pentaphenylene group, a         hexacenylene group, a pentacenylene group, a thiophenylene         group, a furanylene group, a carbazolylene group, an indolylene         group, an isoindolylene group, a benzofuranylene group, a         benzothiophenylene group, a dibenzofuranylene group, a         dibenzothiophenylene group, a benzocarbazolylene group, a         dibenzocarbazolylene group, a dibenzosilolylene group, a         pyridinylene group, an imidazolylene group, a pyrazolylene         group, a thiazolylene group, an isothiazolylene group, an         oxazolylene group, an isoxazolylene group, a thiadiazolylene         group, an oxadiazolylene group, a pyrazinylene group, a         pyrimidinylene group, a pyridazinylene group, a triazinylene         group, a quinolinylene group, an isoquinolinylene group, a         benzoquinolinylene group, a phthalazinylene group, a         naphthyridinylene group, a quinoxalinylene group, a         quinazolinylene group, a cinnolinylene group, a         phenanthridinylene group, an acridinylene group, a         phenanthrolinylene group, a phenazinylene group, a         benzimidazolylene group, an isobenzothiazolylene group, a         benzoxazolylene group, an isobenzoxazolylene group, a         triazolylene group, a tetrazolylene group, an         imidazopyridinylene group, an imidazopyrimidinylene group, and         an azacarbazolylene group; and     -   a phenylene group, a naphthylene group, a fluorenylene group, a         spiro-bifluorenylene group, a benzofluorenylene group, a         dibenzofluorenylene group, a phenanthrenylene group, an         anthracenylene group, a fluoranthenylene group, a         triphenylenylene group, a pyrenylene group, a chrysenylene         group, a perylenylene group, a pentaphenylene group, a         hexacenylene group, a pentacenylene group, a thiophenylene         group, a furanylene group, a carbazolylene group, an indolylene         group, an isoindolylene group, a benzofuranylene group, a         benzothiophenylene group, a dibenzofuranylene group, a         dibenzothiophenylene group, a benzocarbazolylene group, a         dibenzocarbazolylene group, a dibenzosilolylene group, a         pyridinylene group, an imidazolylene group, a pyrazolylene         group, a thiazolylene group, an isothiazolylene group, an         oxazolylene group, an isoxazolylene group, a thiadiazolylene         group, an oxadiazolylene group, a pyrazinylene group, a         pyrimidinylene group, a pyridazinylene group, a triazinylene         group, a quinolinylene group, an isoquinolinylene group, a         benzoquinolinylene group, a phthalazinylene group, a         naphthyridinylene group, a quinoxalinylene group, a         quinazolinylene group, a cinnolinylene group, a         phenanthridinylene group, an acridinylene group, a         phenanthrolinylene group, a phenazinylene group, a         benzimidazolylene group, an isobenzothiazolylene group, a         benzoxazolylene group, an isobenzoxazolylene group, a         triazolylene group, a tetrazolylene group, an         imidazopyridinylene group, an imidazopyrimidinylene group, and         an azacarbazolylene group, each substituted with at least one         selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a         cyano group, a nitro group, an amidino group, a hydrazino group,         a hydrazono group, a C₁-C₂₀ alkyl group, a C₁-C₂₀ alkoxy group,         a phenyl group, a biphenyl group, a terphenyl group, a naphthyl         group, a fluorenyl group, a spiro-bifluorenyl group, a         benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl         group, an anthracenyl group, a fluoranthenyl group, a         triphenylenyl group, a pyrenyl group, a chrysenyl group, a         perylenyl group, a pentaphenyl group, a hexacenyl group, a         pentacenyl group, a thiophenyl group, a furanyl group, a         carbazolyl group, an indolyl group, an isoindolyl group, a         benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl         group, a dibenzothiophenyl group, a benzocarbazolyl group, a         dibenzocarbazolyl group, a dibenzosilolyl group, a pyridinyl         group, an imidazolyl group, a pyrazolyl group, a thiazolyl         group, an isothiazolyl group, an oxazolyl group, an isoxazolyl         group, a thiadiazolyl group, an oxadiazolyl group, a pyrazinyl         group, a pyrimidinyl group, a pyridazinyl group, a triazinyl         group, a quinolinyl group, an isoquinolinyl group, a         benzoquinolinyl group, a phthalazinyl group, a naphthyridinyl         group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl         group, a phenanthridinyl group, an acridinyl group, a         phenanthrolinyl group, a phenazinyl group, a benzimidazolyl         group, an isobenzothiazolyl group, a benzoxazolyl group, an         isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an         imidazopyridinyl group, an imidazopyrimidinyl group, and an         azacarbazolyl group,     -   but embodiments of the present disclosure are not limited         thereto.

In one or more embodiments, xe1 and xe611 to xe613 in Formulae 601 and 601-1 may each independently be 0, 1, or 2.

In one or more embodiments, R₆₀₁ and R₆₁₁ to R₆₁₃ in Formula 601 and 601-1 may each independently be selected from:

-   -   a phenyl group, a biphenyl group, a terphenyl group, a naphthyl         group, a fluorenyl group, a spiro-bifluorenyl group, a         benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl         group, an anthracenyl group, a fluoranthenyl group, a         triphenylenyl group, a pyrenyl group, a chrysenyl group, a         perylenyl group, a pentaphenyl group, a hexacenyl group, a         pentacenyl group, a thiophenyl group, a furanyl group, a         carbazolyl group, an indolyl group, an isoindolyl group, a         benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl         group, a dibenzothiophenyl group, a benzocarbazolyl group, a         dibenzocarbazolyl group, a dibenzosilolyl group, a pyridinyl         group, an imidazolyl group, a pyrazolyl group, a thiazolyl         group, an isothiazolyl group, an oxazolyl group, an isoxazolyl         group, a thiadiazolyl group, an oxadiazolyl group, a pyrazinyl         group, a pyrimidinyl group, a pyridazinyl group, a triazinyl         group, a quinolinyl group, an isoquinolinyl group, a         benzoquinolinyl group, a phthalazinyl group, a naphthyridinyl         group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl         group, a phenanthridinyl group, an acridinyl group, a         phenanthrolinyl group, a phenazinyl group, a benzimidazolyl         group, an isobenzothiazolyl group, a benzoxazolyl group, an         isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an         imidazopyridinyl group, an imidazopyrimidinyl group, and an         azacarbazolyl group;     -   a phenyl group, a biphenyl group, a terphenyl group, a naphthyl         group, a fluorenyl group, a spiro-bifluorenyl group, a         benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl         group, an anthracenyl group, a fluoranthenyl group, a         triphenylenyl group, a pyrenyl group, a chrysenyl group, a         perylenyl group, a pentaphenyl group, a hexacenyl group, a         pentacenyl group, a thiophenyl group, a furanyl group, a         carbazolyl group, an indolyl group, an isoindolyl group, a         benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl         group, a dibenzothiophenyl group, a benzocarbazolyl group, a         dibenzocarbazolyl group, a dibenzosilolyl group, a pyridinyl         group, an imidazolyl group, a pyrazolyl group, a thiazolyl         group, an isothiazolyl group, an oxazolyl group, an isoxazolyl         group, a thiadiazolyl group, an oxadiazolyl group, a pyrazinyl         group, a pyrimidinyl group, a pyridazinyl group, a triazinyl         group, a quinolinyl group, an isoquinolinyl group, a         benzoquinolinyl group, a phthalazinyl group, a naphthyridinyl         group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl         group, a phenanthridinyl group, an acridinyl group, a         phenanthrolinyl group, a phenazinyl group, a benzimidazolyl         group, an isobenzothiazolyl group, a benzoxazolyl group, an         isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an         imidazopyridinyl group, an imidazopyrimidinyl group, and an         azacarbazolyl group, each substituted with at least one selected         from deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano         group, a nitro group, an amidino group, a hydrazino group, a         hydrazono group, a C₁-C₂₀ alkyl group, a C₁-C₂₀ alkoxy group, a         phenyl group, a biphenyl group, a terphenyl group, a naphthyl         group, a fluorenyl group, a spiro-bifluorenyl group, a         benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl         group, an anthracenyl group, a fluoranthenyl group, a         triphenylenyl group, a pyrenyl group, a chrysenyl group, a         perylenyl group, a pentaphenyl group, a hexacenyl group, a         pentacenyl group, a thiophenyl group, a furanyl group, a         carbazolyl group, an indolyl group, an isoindolyl group, a         benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl         group, a dibenzothiophenyl group, a benzocarbazolyl group, a         dibenzocarbazolyl group, a dibenzosilolyl group, a pyridinyl         group, an imidazolyl group, a pyrazolyl group, a thiazolyl         group, an isothiazolyl group, an oxazolyl group, an isoxazolyl         group, a thiadiazolyl group, an oxadiazolyl group, a pyrazinyl         group, a pyrimidinyl group, a pyridazinyl group, a triazinyl         group, a quinolinyl group, an isoquinolinyl group, a         benzoquinolinyl group, a phthalazinyl group, a naphthyridinyl         group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl         group, a phenanthridinyl group, an acridinyl group, a         phenanthrolinyl group, a phenazinyl group, a benzimidazolyl         group, an isobenzothiazolyl group, a benzoxazolyl group, an         isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an         imidazopyridinyl group, an imidazopyrimidinyl group, and an         azacarbazolyl group; and     -   —S(═O)₂(Q₆₀₁) and —P(═O)(Q₆₀₁)(Q₆₀₂), and     -   Q₆₀₁ and Q₆₀₂ may be the same as described herein above.

The electron transport region may include at least one compound selected from Compounds ET1 to ET36, but embodiments of the present disclosure are not limited thereto:

In one or more embodiments, the electron transport region may include at least one selected from 2,9-dimethyl-4,7-diphenyl-1, 10-phenanthroline (BCP), 4,7-diphenyl-1, 10-phenanthroline (Bphen), Alq3, BAlq, 3-(biphenyl-4-yl)-5-(4-tert-butylphenyl)-4-phenyl-4H-1,2,4-triazole (TAZ), and NTAZ:

In one embodiment, the electron transport region may include a phosphine oxide-containing compound (for example, TSPO1 used in the following examples or the like), but embodiments of the present disclosure are not limited thereto. In one embodiment, the phosphine oxide-containing compound may be used in a hole blocking layer in the electron transport region, but embodiments of the present disclosure are not limited thereto.

Thicknesses of the buffer layer, the hole blocking layer, and the electron control layer may each be in a range of about 20 Å to about 1,000 Å, for example, about 30 Å to about 300 Å. When the thicknesses of the buffer layer, the hole blocking layer, and the electron control layer are within these ranges, the electron blocking layer may have excellent electron blocking characteristics or electron control characteristics without a substantial increase in driving voltage.

A thickness of the electron transport layer may be in a range of about 100 Å to about 1,000 Å, for example, about 150 Å to about 500 Å. When the thickness of the electron transport layer is within the range described herein above, the electron transport layer may have suitable or satisfactory electron transport characteristics without a substantial increase in driving voltage.

The electron transport region (for example, the electron transport layer in the electron transport region) may further include, in addition to the materials described herein above, a metal-containing material.

The metal-containing material may include at least one selected from alkali metal complex and alkaline earth-metal complex. The alkali metal complex may include a metal ion selected from a Li ion, a Na ion, a K ion, a Rb ion, and a Cs ion, and the alkaline earth-metal complex may include a metal ion selected from a Be ion, a Mg ion, a Ca ion, a Sr ion, and a Ba ion. A ligand coordinated with the metal ion of the alkali metal complex or the alkaline earth-metal complex may be selected from a hydroxy quinoline, a hydroxy isoquinoline, a hydroxy benzoquinoline, a hydroxy acridine, a hydroxy phenanthridine, a hydroxy phenyloxazole, a hydroxy phenylthiazole, a hydroxy phenyloxadiazole, a hydroxy phenylthiadiazole, a hydroxy phenylpyridine, a hydroxy phenylbenzimidazole, a hydroxy phenylbenzothiazole, a bipyridine, a phenanthroline, and a cyclopentadiene, but embodiments of the present disclosure are not limited thereto.

For example, the metal-containing material may include a Li complex. The Li complex may include, for example, Compound ET-D1 (lithium quinolate, LiQ) or ET-D2:

The electron transport region may include an electron injection layer that facilitates electron injection from the second electrode 190. The electron injection layer may directly contact the second electrode 190.

The electron injection layer may have i) a single-layered structure including a single layer including a single material, ii) a single-layered structure including a single layer including a plurality of different materials, or iii) a multi-layered structure having a plurality of layers including a plurality of different materials.

The electron injection layer may include an alkali metal, an alkaline earth metal, a rare earth metal, an alkali metal compound, an alkaline earth-metal compound, a rare earth metal compound, an alkali metal complex, an alkaline earth-metal complex, a rare earth metal complex, or any combinations thereof.

The alkali metal may be selected from Li, Na, K, Rb, and Cs. In one embodiment, the alkali metal may be Li, Na, or Cs. In one or more embodiments, the alkali metal may be Li or Cs, but embodiments of the present disclosure are not limited thereto.

The alkaline earth metal may be selected from Mg, Ca, Sr, and Ba.

The rare earth metal may be selected from Sc, Y, Ce, Tb, Yb, and Gd.

The alkali metal compound, the alkaline earth-metal compound, and the rare earth metal compound may be selected from oxides and halides (for example, fluorides, chlorides, bromides, or iodides) of the alkali metal, the alkaline earth-metal, and the rare earth metal.

The alkali metal compound may be selected from alkali metal oxides, such as Li₂, Cs₂O, or K₂O, and alkali metal halides, such as LiF, NaF, CsF, KF, LiI, NaI, CsI, or KI. In one embodiment, the alkali metal compound may be selected from LiF, Li₂, NaF, LiI, NaI, CsI, and KI, but embodiments of the present disclosure are not limited thereto.

The alkaline earth-metal compound may be selected from alkaline earth-metal oxides, such as BaO, SrO, CaO, Ba_(x)Sr_(1-x)O (0<x<1), or Ba_(x)Ca_(1-x)O (0<x<1). In one embodiment, the alkaline earth-metal compound may be selected from BaO, SrO, and CaO, but embodiments of the present disclosure are not limited thereto.

The rare earth metal compound may be selected from YbF₃, ScF₃, Sc₂O₃, Y₂O₃, Ce₂O₃, GdF₃, and TbF₃. In one embodiment, the rare earth metal compound may be selected from YbF₃, ScF₃, TbF₃, YbI₃, ScI₃, and TbI₃, but embodiments of the present disclosure are not limited thereto.

The alkali metal complex, the alkaline earth-metal complex, and the rare earth metal complex may include an ion of alkali metal, alkaline earth-metal, and rare earth metal as described herein above, and a ligand coordinated with a metal ion of the alkali metal complex, the alkaline earth-metal complex, or the rare earth metal complex may be selected from hydroxy quinoline, hydroxy isoquinoline, hydroxy benzoquinoline, hydroxy acridine, hydroxy phenanthridine, hydroxy phenyloxazole, hydroxy phenylthiazole, hydroxy diphenyloxadiazole, hydroxy diphenylthiadiazole, hydroxy phenylpyridine, hydroxy phenylbenzimidazole, hydroxy phenylbenzothiazole, bipyridine, phenanthroline, and cyclopentadiene, but embodiments of the present disclosure are not limited thereto.

The electron injection layer may include (or consist of) an alkali metal, an alkaline earth metal, a rare earth metal, an alkali metal compound, an alkaline earth-metal compound, a rare earth metal compound, an alkali metal complex, an alkaline earth-metal complex, a rare earth metal complex, or any combinations thereof, as described herein above. In one or more embodiments, the electron injection layer may further include an organic material. When the electron injection layer further includes an organic material, an alkali metal, an alkaline earth metal, a rare earth metal, an alkali metal compound, an alkaline earth-metal compound, a rare earth metal compound, an alkali metal complex, an alkaline earth-metal complex, a rare earth metal complex, or any combinations thereof may be homogeneously or non-homogeneously dispersed in a matrix including the organic material.

A thickness of the electron injection layer may be in a range of about 1 Å to about 100 Å, for example, about 3 Å to about 90 Å. When the thickness of the electron injection layer is within the range described herein above, the electron injection layer may have suitable or satisfactory electron injection characteristics without a substantial increase in driving voltage.

Second Electrode 190

The second electrode 190 may be on the organic layer 150 having such a structure. The second electrode 190 may be a cathode which is an electron injection electrode, and in this regard, a material for forming the second electrode 190 may be selected from metal, an alloy, an electrically conductive compound, and a combination thereof, which have a relatively low work function.

The second electrode 190 may include at least one selected from lithium (Li), silver (Ag), magnesium (Mg), aluminum (Al), aluminum-lithium (Al—Li), calcium (Ca), magnesium-indium (Mg—In), magnesium-silver (Mg—Ag), ITO, and IZO, but embodiments of the present disclosure are not limited thereto. The second electrode 190 may be a transmissive electrode, a semi-transmissive electrode, or a reflective electrode.

The second electrode 190 may have a single-layered structure, or a multi-layered structure including two or more layers.

Description of FIGS. 2 to 4

FIG. 2 is a schematic view of an organic light-emitting device 20 according to an embodiment. The organic light-emitting device 20 includes a first capping layer 210, the first electrode 110, the organic layer 150, and the second electrode 190, which are sequentially stacked in this stated order. FIG. 3 is a schematic view of an organic light-emitting device 30 according to an embodiment. The organic light-emitting device 30 includes the first electrode 110, the organic layer 150, the second electrode 190, and a second capping layer 220, which are sequentially stacked in this stated order. FIG. 4 is a schematic view of an organic light-emitting device 40 according to an embodiment. The organic light-emitting device 40 includes the first capping layer 210, the first electrode 110, the organic layer 150, the second electrode 190, and the second capping layer 220, which are sequentially stacked in this stated order.

Regarding FIGS. 2 to 4 , the first electrode 110, the organic layer 150, and the second electrode 190 may be understood by referring to the description presented in connection with FIG. 1 .

In the organic layer 150 of each of the organic light-emitting devices 20 and 40, light generated in an emission layer may pass through the first electrode 110 and the first capping layer 210 toward the outside, wherein the first electrode 110 may be a semi-transmissive electrode or a transmissive electrode. In the organic layer 150 of each of the organic light-emitting devices 30 and 40, light generated in an emission layer may pass through the second electrode 190 and the second capping layer 220 toward the outside, wherein the second electrode 190 may be a semi-transmissive electrode or a transmissive electrode.

The first capping layer 210 and the second capping layer 220 may increase external luminescence efficiency according to the principle of constructive interference.

The first capping layer 210 and the second capping layer 220 may each independently be an organic capping layer including an organic material, an inorganic capping layer including an inorganic material, or a composite capping layer including an organic material and an inorganic material. The organic capping layer may include polyethylene terephthalate, polyethylene naphthalate, polycarbonate, polyimide, polyethylene sulfonate, polyoxymethylene, polyarylate, hexamethyldisiloxane, acryl-based resin (e.g., polymethylmethacrylate, polyacrylic acid, etc.), or any combination thereof.

At least one selected from the first capping layer 210 and the second capping layer 220 may each independently include at least one material selected from carbocyclic compounds, heterocyclic compounds, amine-based compounds, porphyrine derivatives, phthalocyanine derivatives, a naphthalocyanine derivatives, alkali metal complexes, and alkaline earth-based complexes. The carbocyclic compound, the heterocyclic compound, and the amine-based compound may be optionally substituted with a substituent containing at least one element selected from O, N, S, Se, Si, F, Cl, Br, and I.

In one embodiment, at least one selected from the first capping layer 210 and the second capping layer 220 may each independently include an amine-based compound.

In one embodiment, at least one selected from the first capping layer 210 and the second capping layer 220 may each independently include the compound represented by Formula 201 or the compound represented by Formula 202.

In one or more embodiments, at least one selected from the first capping layer 210 and the second capping layer 220 may each independently include a compound selected from Compounds HT28 to HT33 and Compounds CP1 to CP5, but embodiments of the present disclosure are not limited thereto:

Hereinbefore, the organic light-emitting device according to an embodiment has been described in connection with FIGS. 1 to 4 , but embodiments of the present disclosure are not limited thereto.

Layers constituting the hole transport region, an emission layer, and layers constituting the electron transport region may be formed in a certain region by using one or more suitable methods selected from vacuum deposition, spin coating, casting, Langmuir-Blodgett (LB) deposition, ink-jet printing, laser-printing, and laser-induced thermal imaging.

When layers constituting the hole transport region, an emission layer, and layers constituting the electron transport region are formed by vacuum deposition, the deposition may be performed at a deposition temperature of about 100° C. to about 500° C., a vacuum degree of about 10⁻⁸ torr to about 10⁻³ torr, and a deposition speed of about 0.01 Å/sec to about 100 Å/sec by taking into account a material to be included in a layer to be formed, and the structure of a layer to be formed.

When layers constituting the hole transport region, an emission layer, and layers constituting the electron transport region are formed by spin coating, the spin coating may be performed at a coating speed of about 2,000 rpm to about 5,000 rpm and at a heat treatment temperature of about 80° C. to 200° C. by taking into account a material to be included in a layer to be formed, and the structure of a layer to be formed.

Apparatus

The organic light-emitting device may be included in various suitable apparatuses. For example, a light-emitting apparatus, an authentication apparatus, or an electronic apparatus, which includes the organic light-emitting device, may be provided.

The light-emitting apparatus may further include, in addition to the organic light-emitting device, a thin film transistor including a source electrode and a drain electrode. One of the source electrode and the drain electrode of the thin film transistor may be in electrical contact with one of the first electrode and the second electrode of the organic light-emitting device. The light-emitting apparatus may be used as various suitable displays, light sources, and/or the like.

The authentication apparatus may be, for example, a biometric authentication apparatus for authenticating an individual by using biometric information of a biometric body (for example, a fingertip, a pupil, and/or the like).

The authentication apparatus may further include, in addition to the organic light-emitting device, a biometric information collector.

The electronic apparatus may be applied to personal computers (for example, a mobile personal computer), mobile phones, digital cameras, electronic organizers, electronic dictionaries, electronic game machines, medical instruments (for example, electronic thermometers, sphygmomanometers, blood glucose meters, pulse measurement devices, pulse wave measurement devices, electrocardiogram (ECG) displays, ultrasonic diagnostic devices, and/or endoscope displays), fish finders, various suitable measuring instruments, meters (for example, meters for a vehicle, an aircraft, and a vessel), projectors, and/or the like, but embodiments of the present disclosure are not limited thereto.

General Definition of at Least Some of the Substituents

The term “C₁-C₆₀ alkyl group,” as used herein, refers to a linear or branched aliphatic saturated hydrocarbon monovalent group having 1 to 60 carbon atoms, and examples thereof include a methyl group, an ethyl group, a propyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a pentyl group, an isoamyl group, and a hexyl group. The term “C₁-C₆₀ alkylene group,” as used herein, refers to a divalent group having substantially the same structure as the C₁-C₆₀ alkyl group.

The term “C₂-C₆₀ alkenyl group,” as used herein, refers to a hydrocarbon group having at least one carbon-carbon double bond at a main chain (e.g., in the middle) or at a terminal end (e.g., the terminus) of the C₂-C₆₀ alkyl group, and examples thereof include an ethenyl group, a propenyl group, and a butenyl group. The term “C₂-C₆₀ alkenylene group,” as used herein, refers to a divalent group having substantially the same structure as the C₂-C₆₀ alkenyl group.

The term “C₂-C₆₀ alkynyl group,” as used herein, refers to a hydrocarbon group having at least one carbon-carbon triple bond at a main chain (e.g., in the middle) or at a terminal end (e.g., the terminus) of the C₂-C₆₀ alkyl group, and examples thereof include an ethynyl group, and a propynyl group. The term “C₂-C₆₀ alkynylene group,” as used herein, refers to a divalent group having substantially the same structure as the C₂-C₆₀ alkynyl group.

The term “C₁-C₆₀ alkoxy group,” as used herein, refers to a monovalent group represented by —OA₁₀₁ (wherein A₁₀₁ is the C₁-C₆₀ alkyl group), and examples thereof include a methoxy group, an ethoxy group, and an isopropyloxy group.

The term “C₃-C₁₀ cycloalkyl group,” as used herein, refers to a monovalent saturated hydrocarbon monocyclic group having 3 to 10 carbon atoms, and examples thereof include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, and a cycloheptyl group. The term “C₃-C₁₀ cycloalkylene group,” as used herein, refers to a divalent group having substantially the same structure as the C₃-C₁₀ cycloalkyl group.

The term “C₁-C₁₀ heterocycloalkyl group,” as used herein, refers to a monovalent monocyclic group having at least one heteroatom selected from N, O, Si, P, and S as a ring-forming atom and 1 to 10 carbon atoms, and examples thereof include a 1,2,3,4-oxatriazolidinyl group, a tetrahydrofuranyl group, and a tetrahydrothiophenyl group. The term “C₁-C₁₀ heterocycloalkylene group,” as used herein, refers to a divalent group having substantially the same structure as the C₁-C₁₀ heterocycloalkyl group.

The term “C₃-C₁₀ cycloalkenyl group,” as used herein, refers to a monovalent monocyclic group that has 3 to 10 carbon atoms and at least one carbon-carbon double bond in the ring thereof and no aromaticity (e.g., is not aromatic), and examples thereof include a cyclopentenyl group, a cyclohexenyl group, and a cycloheptenyl group. The term “C₃-C₁₀ cycloalkenylene group,” as used herein, refers to a divalent group having substantially the same structure as the C₃-C₁₀ cycloalkenyl group.

The term “C₁-C₁₀ heterocycloalkenyl group,” as used herein, refers to a monovalent monocyclic group that has at least one heteroatom selected from N, O, Si, P, and S as a ring-forming atom, 1 to 10 carbon atoms, and at least one carbon-carbon double bond in its ring. Non-limiting examples of the C₁-C₁₀ heterocycloalkenyl group include a 4,5-dihydro-1,2,3,4-oxatriazolyl group, a 2,3-dihydrofuranyl group, and a 2,3-dihydrothiophenyl group. The term “C₁-C₁₀ heterocycloalkenylene group,” as used herein, refers to a divalent group having substantially the same structure as the C₁-C₁₀ heterocycloalkenyl group.

The term “C₆-C₆₀ aryl group,” as used herein, refers to a monovalent group having a carbocyclic aromatic system having 6 to 60 carbon atoms, and the term “C₆-C₆₀ arylene group,” as used herein, refers to a divalent group having a carbocyclic aromatic system having 6 to 60 carbon atoms. Non-limiting examples of the C₆-C₆₀ aryl group include a phenyl group, a naphthyl group, an anthracenyl group, a phenanthrenyl group, a pyrenyl group, and a chrysenyl group. When the C₆-C₆₀ aryl group and the C₆-C₆₀ arylene group each include two or more rings, the rings may be fused to each other (e.g., combined together).

The term “C₁-C₆₀ heteroaryl group,” as used herein, refers to a monovalent group having a carbocyclic aromatic system that has at least one heteroatom selected from N, O, Si, P, and S as a ring-forming atom, in addition to 1 to 60 carbon atoms. The term “C₁-C₆₀ heteroarylene group,” as used herein, refers to a divalent group having a carbocyclic aromatic system that has at least one heteroatom selected from N, O, Si, P, and S as a ring-forming atom, in addition to 1 to 60 carbon atoms. Non-limiting examples of the C₁-C₆₀ heteroaryl group include a pyridinyl group, a pyrimidinyl group, a pyrazinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, and an isoquinolinyl group. When the C₁-C₆₀ heteroaryl group and the C₁-C₆₀ heteroarylene group each include two or more rings, the rings may be condensed with each other (e.g., combined together).

The term “C₆-C₆₀ aryloxy group,” as used herein, refers to —OA₁₀₂ (wherein A₁₀₂ is the C₆-C₆₀ aryl group), and the term “C₆-C₆₀ arylthio group,” as used herein, indicates —SA₁₀₃ (wherein A₁₀₃ is the C₆-C₆₀ aryl group).

The term “monovalent non-aromatic condensed polycyclic group,” as used herein, refers to a monovalent group (for example, having 8 to 60 carbon atoms) having two or more rings condensed with each other (e.g., combined together), only carbon atoms as ring-forming atoms, and no aromaticity in its entire molecular structure (e.g., is not aromatic). An example of the monovalent non-aromatic condensed polycyclic group is a fluorenyl group. The term “divalent non-aromatic condensed polycyclic group,” as used herein, refers to a divalent group having substantially the same structure as the monovalent non-aromatic condensed polycyclic group.

The term “monovalent non-aromatic condensed heteropolycyclic group,” as used herein, refers to a monovalent group (for example, having 1 to 60 carbon atoms) having two or more rings condensed to each other (e.g., combined together), at least one heteroatom selected from N, O, Si, P, and S, other than carbon atoms, as a ring-forming atom, and no aromaticity in its entire molecular structure (e.g., is not aromatic). An example of the monovalent non-aromatic condensed heteropolycyclic group is a carbazolyl group. The term “divalent non-aromatic condensed heteropolycyclic group,” as used herein, refers to a divalent group having substantially the same structure as the monovalent non-aromatic condensed heteropolycyclic group.

The term “C₄-C₆₀ carbocyclic group,” as used herein, refers to a monocyclic or polycyclic group having 4 to 60 carbon atoms in which a ring-forming atom is a carbon atom only. The term “C₄-C₆₀ carbocyclic group,” as used herein, refers to an aromatic carbocyclic group or a non-aromatic carbocyclic group. The C₄-C₆₀ carbocyclic group may be a ring, such as benzene, a monovalent group, such as a phenyl group, or a divalent group, such as a phenylene group. In one or more embodiments, depending on the number of substituents connected to the C₄-C₆₀ carbocyclic group, the C₄-C₆₀ carbocyclic group may be a trivalent group or a quadrivalent group.

The term “C₁-C₆₀ heterocyclic group,” as used herein, refers to a group having substantially the same structure as the C₄-C₆₀ carbocyclic group, except that as a ring-forming atom, at least one heteroatom selected from N, O, Si, P, and S is used in addition to carbon (the number of carbon atoms may be in a range of 1 to 60).

In the present specification, at least one substituent of the substituted C₄-C₆₀ carbocyclic group, the substituted C₁-C₆₀ heterocyclic group, the substituted C₃-C₁₀ cycloalkylene group, the substituted C₁-C₁₀ heterocycloalkylene group, the substituted C₃-C₁₀ cycloalkenylene group, the substituted C₁-C₁₀ heterocycloalkenylene group, the substituted C₆-C₆₀ arylene group, the substituted C₁-C₆₀ heteroarylene group, the substituted divalent non-aromatic condensed polycyclic group, the substituted divalent non-aromatic condensed heteropolycyclic group, the substituted C₁-C₆₀ alkyl group, the substituted C₂-C₆₀ alkenyl group, the substituted C₂-C₆₀ alkynyl group, the substituted C₁-C₆₀ alkoxy group, the substituted C₃-C₁₀ cycloalkyl group, the substituted C₁-C₁₀ heterocycloalkyl group, the substituted C₃-C₁₀ cycloalkenyl group, the substituted C₁-C₁₀ heterocycloalkenyl group, the substituted C₆-C₆₀ aryl group, the substituted C₆-C₆₀ aryloxy group, the substituted C₆-C₆₀ arylthio group, the substituted C₁-C₆₀ heteroaryl group, the substituted monovalent non-aromatic condensed polycyclic group, and the substituted monovalent non-aromatic condensed heteropolycyclic group may be selected from:

-   -   deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a         nitro group, an amidino group, a hydrazino group, a hydrazono         group, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀         alkynyl group, and a C₁-C₆₀ alkoxy group;     -   a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl         group, and a C₁-C₆₀ alkoxy group, each substituted with at least         one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group,         a cyano group, a nitro group, an amidino group, a hydrazino         group, a hydrazono group, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀         heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀         heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy         group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a         monovalent non-aromatic condensed polycyclic group, a monovalent         non-aromatic condensed heteropolycyclic group,         —Si(Q₁₁)(Q₁₂)(Q₁₃), —N(Q₁₁)(Q₁₂), —B(Q₁₁)(Q₁₂), —C(═O)(Q₁₁),         —S(═O)₂(Q₁₁), and —P(═O)(Q₁₁)(Q₁₂);     -   a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a         C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a         C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio         group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic         condensed polycyclic group, and a monovalent non-aromatic         condensed heteropolycyclic group;     -   a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a         C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a         C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio         group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic         condensed polycyclic group, and a monovalent non-aromatic         condensed heteropolycyclic group, each substituted with at least         one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group,         a cyano group, a nitro group, an amidino group, a hydrazino         group, a hydrazono group, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl         group, a C₂-C₆₀ alkynyl group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀         cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀         cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀         aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a         C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed         polycyclic group, a monovalent non-aromatic condensed         heteropolycyclic group, —Si(Q₂₁)(Q₂₂)(Q₂₃), —N(Q₂₁)(Q₂₂),         —B(Q₂₁)(Q₂₂), —C(═O)(Q₂₁), —S(═O)₂(Q₂₁), and —P(═O)(Q₂₁)(Q₂₂);         and     -   —Si(Q₃₁)(Q₃₂)(Q₃₃), —N(Q₃₁)(Q₃₂), —B(Q₃₁)(Q₃₂), —C(═O)(Q₃₁),         —S(═O)₂(Q₃₁), and —P(═O)(Q₃₁)(Q₃₂), and     -   Q₁₁ to Q₁₃, Q₂₁ to Q₂₃, and Q₃₁ to Q₃₃ may each independently be         selected from hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl         group, a cyano group, a nitro group, an amidino group, a         hydrazino group, a hydrazono group, a C₁-C₆₀ alkyl group, a         C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a C₁-C₆₀ alkoxy         group, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl         group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl         group, a C₆-C₆₀ aryl group, a C₁-C₆₀ heteroaryl group, a         monovalent non-aromatic condensed polycyclic group, a monovalent         non-aromatic condensed heteropolycyclic group, a C₁-C₆₀ alkyl         group substituted with at least one selected from deuterium, —F,         and a cyano group, a C₆-C₆₀ aryl group substituted with at least         one selected from deuterium, —F, and a cyano group, a biphenyl         group, and a terphenylgroup.

The term “Ph,” as used herein, refers to a phenyl group, the term “Me,” as used herein, refers to a methyl group, the term “Et,” as used herein, refers to an ethyl group, the term “ter-Bu” or “Bu^(t),” as used herein, refers to a tert-butyl group, and the term “OMe,” as used herein, refers to a methoxy group.

The term “biphenyl group,” as used herein, refers to “a phenyl group substituted with a phenyl group”. In other words, the “biphenyl group” is a substituted phenyl group having a C₆-C₆₀ aryl group as a substituent.

The term “terphenyl group” as used herein refers to “a phenyl group substituted with a biphenyl group.” In other words, the “terphenyl group” is a phenyl group having, as a substituent, a C₆-C₆₀ aryl group substituted with a C₆-C₆₀ aryl group.

* and *′, as used herein, unless defined otherwise, each refer to a binding site to a neighboring atom in a corresponding formula.

Hereinafter, a compound according to embodiments and an organic light-emitting device according to embodiments will be described in more detail with reference to Synthesis Examples and Examples. The wording “B was used instead of A” used in describing Synthesis Examples refers to that an identical molar equivalent of B was used in place of A.

EXAMPLES Synthesis Example: Synthesis of Compound

Synthesis of Compound 1-4

4,9-dibromoquinolino[7,8-h]quinoline (3.9 g, 10 mmol), 2,4-diphenyl-6-[4-(4, 4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-s-triazine (5.0 g, 11 mmol), K₂CO₃ (2.8 g, 20 mmol), and Pd(PPh₃)₄ (0.41 g, 0.35 mmol) were added to a schlenk tube, dried in a vacuum state for 2 hours, and then dissolved in tetrahydrofuran (THF) (100 mL). N₂-purged anhydrous EtOH (20 mL) was added thereto and stirred at a temperature of 80° C. for 24 hours in a nitrogen atmosphere. The reaction mixture was cooled to room temperature, and a solvent was removed therefrom under reduced pressure. The resultant was washed by using an excess of dichloromethane (DCM) and distilled water, and an organic layer was separated therefrom. The separated organic layer was dried by using MgSO₄ and purified by column chromatography (DCM/hexane (1:1, v/v)) to obtain Intermediate 1-4-A (3.1 g, 5.0 mmol, yield: 50%).

Intermediate 1-4-A (6.2 g, 10 mmol), phenylboronic acid (1.5 g, 12 mmol), K₂CO₃ (1.4 g, 10 mmol), and Pd(PPh₃)₄ (0.41 g, 0.35 mmol) were added to a schlenk tube, dried in a vacuum state for 2 hours, and then dissolved in dimethylformamide (DMF) (100 mL). N₂-purged anhydrous EtOH (20 mL) was added thereto and stirred at a temperature of 100° C. for 24 hours in a nitrogen atmosphere. The reaction mixture was cooled to room temperature, and a solvent was removed therefrom under reduced pressure. The resultant was washed by using an excess of DCM and distilled water, and an organic layer was separated therefrom. The separated organic layer was dried by using MgSO₄ and purified by column chromatography (DCM) to obtain Compound 1-4 (4.8 g, 7.8 mmol, yield: 78%).

Synthesis of Compound-2-3

3.8-dibromo-1,10-phenanthroline (3.4 g, 10 mmol), 2,4-diphenyl-6-[4-(4,4,5, 5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-s-triazine (5.0 g, 11 mmol), K₂CO₃ (2.8 g, 20 mmol), and Pd(PPh₃)₄ (0.41 g, 0.35 mmol) were added to a schlenk tube, dried in a vacuum state for 2 hours, and then dissolved in DMF (100 mL). N₂-purged anhydrous EtOH (20 mL) was added thereto and stirred at a temperature of 100° C. for 24 hours in a nitrogen atmosphere. The reaction mixture was cooled to room temperature, and a solvent was removed therefrom under reduced pressure. The resultant was washed by using an excess of DCM and distilled water, and an organic layer was separated therefrom. The separated organic layer was dried by using MgSO₄ and purified by column chromatography (DCM/hexane (10:1, v/v)) to obtain Intermediate 2-3-A (4.4 g, 7.7 mmol, yield: 77%).

Intermediate 2-3-A (5.7 g, 10 mmol), phenylboronic acid (1.5 g, 12 mmol), K₂CO₃ (1.4 g, 10 mmol), and Pd(PPh₃)₄ (0.41 g, 0.35 mmol) were added to a schlenk tube, dried in a vacuum state for 2 hours, and then dissolved in THF (100 mL). N₂-purged anhydrous EtOH (20 mL) was added thereto and stirred at a temperature of 80° C. for 24 hours in a nitrogen atmosphere. The reaction mixture was cooled to room temperature, and a solvent was removed therefrom under reduced pressure. The resultant was washed by using an excess of chloroform and distilled water, and an organic layer was separated therefrom. The separated organic layer was dried by using MgSO₄ and purified by column chromatography (chloroform) to obtain Compound 2-3 (4.1 g, 7.3 mmol, yield: 73%).

Synthesis of Compound 2-7

Intermediate 2-3-A (5.7 g, 10 mmol) was dissolved in anhydrous toluene (50 mL)/THF (10 mL) in a nitrogen atmosphere, and n-BuLi (5 mL, 1.2 equiv. 2.5 M in hexane) was slowly added thereto at a temperature of −78° C. The reaction mixture was stirred at a temperature of −78° C. for 1 hour, and trimethylborate (1.2 mmol) was added thereto. HCl (12 mL, 2M solution) was added thereto, and the solution was heated to room temperature. A separated organic layer was washed by using distilled water and brine solution. The solution was dried by using MgSO₄, and a solvent was removed therefrom under reduced pressure. A product obtained therefrom was washed several times by using hot n-hexane to obtain Intermediate 2-7-A (3.7 g, 6.9 mmol, yield: 69%).

Intermediate 2-7-A (5.3 g, 10 mmol), 6-bromo-4-phenylbenzofuro[3,2-b]pyridine (3.2 g, 10 mmol), K₂CO₃ (2.8 g, 20 mmol), and Pd(PPh₃)₄ (0.41 g, 0.35 mmol) were added to a schlenk tube, dried in a vacuum state for 2 hours, and then dissolved in 1,4-dioxane (100 mL). N₂-purged anhydrous MeOH (20 mL) was added thereto and stirred at a temperature of 130° C. for 48 hours in a nitrogen atmosphere. The reaction mixture was cooled to room temperature, and a solvent was removed therefrom under reduced pressure. The resultant was washed by using an excess of chloroform and distilled water, and an organic layer was separated therefrom. The separated organic layer was dried by using MgSO₄ and purified by column chromatography (chloroform) to obtain Compound 2-7 (2.9 g, 4.0 mmol, yield: 40%).

Synthesis of Compound 2-5

1,4-dibromonaphthalene (2.9 g, 10 mmol), 2,4-diphenyl-6-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-s-triazine (5.0 g, 11 mmol), K₂CO₃ (2.8 g, 20 mmol), and Pd(PPh₃)₄ (0.41 g, 0.35 mmol) were added to a schlenk tube, dried in a vacuum state for 2 hours, and then dissolved in DMF (100 mL). N₂-purged anhydrous EtOH (20 mL) was added thereto and stirred at a temperature of 100° C. for 24 hours in a nitrogen atmosphere. The reaction mixture was cooled to room temperature, and a solvent was removed therefrom under reduced pressure. The resultant was washed by using an excess of DCM and distilled water, and an organic layer was separated therefrom. The separated organic layer was dried by using MgSO₄ and purified by column chromatography (DCM/hexane (2:1, v/v)) to obtain Intermediate 2-5-A (3.5 g, 6.8 mmol yield: 68%).

Intermediate 2-5-A (5.1 g, 10 mmol), (8-cyano-1,10-phenanthrolin-3-yl)boronic acid (2.7 g, 11 mmol), K₂CO₃ (2.8 g, 20 mmol), and Pd(PPh₃)₄ (0.41 g, 0.35 mmol) were added to a schlenk tube, dried in a vacuum state for 2 hours, and then dissolved in DMF (100 mL). N₂-purged anhydrous EtOH (20 mL) was added thereto and stirred at a temperature of 100° C. for 48 hours in a nitrogen atmosphere. The reaction mixture was cooled to room temperature, and a solvent was removed therefrom under reduced pressure. The resultant was washed by using an excess of chloroform and distilled water, and an organic layer was separated therefrom. The separated organic layer was dried by using MgSO₄ and purified by column chromatography (chloroform) to obtain Compound 2-5 (4.1 g, 6.4 mmol, yield: 64%).

Synthesis of Compound 6-1

5,5′-dibromo-2,2′-bipyrimidine (3.2 g, 10 mmol), phenylboronic acid (1.5 g, 12 mmol), K₂CO₃ (1.4 g, 10 mmol), and Pd(PPh₃)₄ (0.41 g, 0.35 mmol) were added to a schlenk tube, dried in a vacuum state for 2 hours, and then dissolved in THF (100 mL). N₂-purged anhydrous EtOH (20 mL) was added thereto and stirred at a temperature of 80° C. for 24 hours in a nitrogen atmosphere. The reaction mixture was cooled to room temperature, and a solvent was removed therefrom under reduced pressure. The resultant was washed by using an excess of DCM and distilled water, and an organic layer was separated therefrom. The separated organic layer was dried by using MgSO₄ and purified by column chromatography (dichloromethane) to obtain Intermediate 6-1-A (2.4 g, 7.7 mmol, yield: 77%).

Intermediate 6-1-A (3.1 g, 10 mmol), 2,4-diphenyl-6-[4-(4,4,5,5-tetramethyl-1, 3,2-dioxaborolan-2-yl)phenyl]-s-triazine (5.0 g, 11 mmol), K₂CO₃ (2.8 g, 20 mmol), and Pd(PPh₃)₄ (0.41 g, 0.35 mmol) were added to a schlenk tube, dried in a vacuum state for 2 hours, and then dissolved in 1,4-dioxane (100 mL). N₂-purged anhydrous EtOH (20 mL) was added thereto and stirred at a temperature of 120° C. for 24 hours in a nitrogen atmosphere. The reaction mixture was cooled to room temperature, and a solvent was removed therefrom under reduced pressure. The resultant was washed by using an excess of chloroform and distilled water, and an organic layer was separated therefrom. The separated organic layer was dried by using MgSO₄ and purified by column chromatography (chloroform/hexane (5:1, v/v)) to obtain Compound 6-1 (2.9 g, 5.4 mmol, yield: 54%).

Synthesis of Compound 7-10

2,7-dibromodipyrazino[2,3-f:2′,3′-h]quinoxaline (3.9 g, 10 mmol), phenylboronic acid (1.5 g, 12 mmol), K₂CO₃ (2.8 g, 20 mmol), and Pd(PPh₃)₄ (0.41 g, 0.35 mmol) were added to a schlenk tube, dried in a vacuum state for 2 hours, and then dissolved in DMF (100 mL). N₂-purged anhydrous EtOH (20 mL) was added thereto and stirred at a temperature of 100° C. for 24 hours in a nitrogen atmosphere. The reaction mixture was cooled to room temperature, and a solvent was removed therefrom under reduced pressure. The resultant was washed by using an excess of DCM and distilled water, and an organic layer was separated therefrom. The separated organic layer was dried by using MgSO₄ and purified by column chromatography (DCM) to obtain Intermediate 7-10-A (1.8 g, 4.6 mmol, yield: 46%).

Intermediate 7-10-A (3.9 g, 10 mmol), 2,4-diphenyl-6-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-s-triazine (5.0 g, 11 mmol), K₂CO₃ (2.8 g, 20 mmol), and Pd(PPh₃)₄ (0.41 g, 0.35 mmol) were added to a schlenk tube, dried in a vacuum state for 2 hours, and then dissolved in 1,4-dioxane (100 mL). N₂-purged anhydrous EtOH (20 mL) was added thereto and stirred at a temperature of 120° C. for 48 hours in a nitrogen atmosphere. The reaction mixture was cooled to room temperature, and a solvent was removed therefrom under reduced pressure. The resultant was washed by using an excess of DCM and distilled water, and an organic layer was separated therefrom. The separated organic layer was dried by using MgSO₄ and purified by column chromatography (DCM) to obtain Compound 7-10 (3.5 g, 5.7 mmol, yield: 57%).

¹H NMR of each of Compounds synthesized according to Synthesis Examples is shown in Table 1.

Synthesis methods of compounds other than Compounds shown in Table 1 may also be easily recognized by those of ordinary skill in the art upon referring to the synthesis mechanisms and source materials described herein above.

TABLE 1 Compound ¹H NMR (DMSO-d₆, 500 MHz) 1-4 7.15(d, 2H), 7.25(d, 2H), 7.41-7.50(m,9H), 7.79-7.82(dd, 4H), 7.96(d, 2H), 8.12(d, 2H), 8.36(d, 4H), 8.87 (d, 2H) 2-3 7.25(d, 2H), 7.46-7.50(m,11H), 7.91- 7.96(m, 3H), 8.12(d, 1H), 8.20(s, 2H), 8.40(d, 4H) 2-5 7.24(d, 2H), 7.46-7.52(m,8H), 7.84- 7.96(m, 4H), 8.06-8.12(dd, 2H), 8.20(s, 1H), 8.26 (s, 1H), 8.36 (d, 4H), 8.81(s, 1H), 8.95-9.02(dd, 2H), 9.40 (s, 1H) 2-7 7.25(d, 2H), 7.41-7.51(m, 12H), 7.80 (d, 1H), 7.91-8.02(m, 5H), 8.12(d, 1H)), 8.19(s, 1H), 8.26 (s, 1H), 8.36 (d, 4H), 8.61(s, 1H) 6-1 7.20(d, 2H), 7.46-7.51(m, 11H), 7.96 (d, 2H), 8.32 (d, 4H), 9.61(s, 4H) 7-10 7.49-7.59(m, 9H), 7.94-8.00 (dd, 6H), 8.23 (s, 1H), 8.26 (d, 2H), 8.75 (s, 4H), 8.86 (d, 2H)

Simulation Evaluation

HOMO, LUMO, triplet energy level, singlet energy level, diploe, and oscillator strength (OSC) of Compounds 1-1 to 8-1 according to one or more embodiments, TPBi, and Compounds 101, 102, 103, and 104 were obtained a simulation (name: Gaussian, version: B3LYP/6-31 G*; e.g., the simulation included density functional theory calculations performed utilizing a B3LYP hybrid functional and a 6-31 G* basis set conducted utilizing the Gaussian software package) and compared, and results thereof are shown in Table 2.

TABLE 2 Com- HOMO LUMO Eg Triplet Singlet pound (eV) (eV) (eV) (eV) (eV) dipole OSC 1-1 −5.76 −2.13 3.63 2.45 2.85 2.34 f = 0.0002 1-2 −5.76 −2.03 3.73 2.46 2.99 2.26 f = 0.0175 1-3 −5.87 −2.15 3.72 2.46 2.99 4.11 f = 0.0090 1-4 −5.77 −2.02 3.75 2.46 2.99 2.19 f = 0.0228 2-1 −5.81 −2.06 3.74 2.47 3.15 4.69 f = 0.3850 2-2 −5.71 −1.94 3.77 2.49 3.16 3.03 f = 0.4203 2-3 −6.02 −2.09 3.93 2.60 3.23 3.08 f = 1.1958 2-4 −6.14 −2.21 3.92 2.62 3.22 4.67 f = 0.8183 2-5 −6.15 −2.48 3.67 2.51 3.23 7.02 f = 0.5377 2-6 −6.06 −2.24 3.81 2.60 3.10 3.46 f = 0.7561 2-7 −5.98 −2.12 3.87 2.60 3.11 3.01 f = 0.9681 3-1 −5.89 −2.08 3.82 2.62 3.24 3.27 f = 1.0522 3-2 −6.00 −2.19 3.80 2.64 3.23 4.88 f = 0.8623 4-1 −6.16 −2.51 3.65 2.40 2.91 0.60 f = 1.3958 4-2 −6.34 −2.61 3.73 2.48 2.91 2.58 f = 1.0225 5-1 −5.98 −2.07 3.91 2.67 3.53 2.93 f = 1.5003 5-2 −6.12 −2.19 3.94 2.74 3.24 4.65 f = 0.7465 6-1 −6.18 −2.27 3.91 2.65 3.13 0.04 f = 0.0872 6-2 −6.30 −2.40 3.90 2.69 3.10 2.03 f = 0.0646 7-1 −5.68 −1.80 3.88 2.44 3.03 0.74 f = 0.0003 7-2 −5.71 −1.67 4.04 2.50 3.29 3.20 f = 0.6133 7-3 −5.91 −1.80 4.11 2.69 3.27 3.93 f = 0.9819 7-4 −6.02 −2.40 3.62 2.49 2.97 1.97 f = 0.0113 7-5 −5.97 −1.79 4.18 2.76 3.28 3.62 f = 1.3198 7-6 −6.04 −2.11 3.93 2.75 3.19 1.86 f = 0.0020 7-7 −5.66 −1.86 3.80 2.41 3.01 1.74 f = 0.0310 7-8 −5.67 −1.79 3.87 2.44 3.28 4.56 f = 0.7059 7-9 −6.00 −1.93 4.07 2.63 3.24 1.85 f = 1.0795 7-10 −6.14 −2.42 3.72 2.48 2.92 1.48 f = 1.1623 7-11 −5.97 −1.93 4.04 2.72 3.33 1.73 f = 1.3297 7-12 −6.15 −2.19 3.96 2.67 3.13 1.90 f = 0.0849 8-1 −6.08 −2.30 3.78 2.63 3.40 4.15 f = 1.4309 TPBi −5.89 −1.51 4.38 2.79 3.74 1.04 f = 0.0031 100 −5.90 −2.27 3.62 2.17 3.19 0.72 f = 0.0379 101 −6.33 −2.30 4.03 2.72 3.64 0.06 f = 0.0139 102 −6.25 −2.30 3.95 2.72 3.42 1.26 f = 0.0002 103 −5.79 −2.23 3.57 2.28 3.12 1.19 f = 0.0494

(in Table 2, “Eg” indicates a gap between HOMO and LUMO.)

From Table 2, it can be seen that Compounds 1-1 to 8-1 according to one or more embodiments have stronger oscillator strength than TPBi and Compounds 100, 101, 102, and 103. For the dipole value, it can be seen that Compounds 1-1 to 8-1 according to one or more embodiments are more polar than TPBi and Compounds 100, 101, 102, and 103. Therefore, the dipole moments of Compounds 1-1 to 8-1 according to one or more embodiments are expected to be located in the plane forming the molecules. This may be expected to have a more constant (e.g., more uniform) orientation than TPBi and Compounds 100, 102, and 103 in the molecular arrangement during deposition.

Manufacture of Organic Light-Emitting Device

Comparative Example 1

As an anode, a Corning 15 Ω/cm² (1,200 Å) ITO glass substrate was cut to a size of 50 mm×50 mm×0.5 mm, sonicated with isopropyl alcohol and pure water each for 5 minutes, and then cleaned by exposure to ultraviolet rays and ozone for 30 minutes. Then, the ITO glass substrate was provided to a vacuum deposition apparatus.

An existing material (HAT-CN) was vacuum-deposited on the ITO glass substrate to form a hole injection layer having a thickness of 100 Å, and a hole transport compound TAPC was vacuum-deposited on the hole injection layer to form a hole transport layer having a thickness of 300 Å.

mCP and TPBe were co-deposited on the hole transport layer at a weight ratio of 94:6 wt % to form an emission layer having a thickness of 300 Å.

T2T was deposited on the emission layer to form a hole blocking layer having a thickness of 100 Å, TPBi was deposited on the hole blocking layer to form an electron transport layer having a thickness of 550 Å.

LiF was deposited on the electron transport layer to form an electron injection layer having a thickness of 8 Å, and Al was deposited on the electron injection layer to form an electrode having a thickness of 1,000 Å.

Comparative Example 2

An organic light-emitting device was manufactured in substantially the same manner as in Comparative Example 1, except that Compound 100 was used instead of TPBi in forming an electron transport layer.

Comparative Example 3

An organic light-emitting device was manufactured in substantially the same manner as in Comparative Example 1, except that Compound 101 was used instead of TPBi in forming an electron transport layer.

Comparative Example 4

An organic light-emitting device was manufactured in substantially the same manner as in Comparative Example 1, except that Compound 102 was used instead of TPBi in forming an electron transport layer.

Comparative Example 5

An organic light-emitting device was manufactured in substantially the same manner as in Comparative Example 1, except that Compound 103 was used instead of TPBi in forming an electron transport layer.

Example 1

An organic light-emitting device was manufactured in substantially the same manner as in Comparative Example 1, except that Compound 1-4 was used instead of TPBi in forming an electron transport layer.

Example 2

An organic light-emitting device was manufactured in substantially the same manner as in Comparative Example 1, except that Compound 2-3 was used instead of TPBi in forming an electron transport layer.

Example 3

An organic light-emitting device was manufactured in substantially the same manner as in Comparative Example 1, except that Compound 2-7 was used instead of TPBi in forming an electron transport layer.

Example 4

An organic light-emitting device was manufactured in substantially the same manner as in Comparative Example 1, except that Compound 6-1 was used instead of TPBi in forming an electron transport layer.

Example 5

An organic light-emitting device was manufactured in substantially the same manner as in Comparative Example 1, except that Compound 7-10 was used instead of TPBi in forming an electron transport layer.

Example 6

An organic light-emitting device was manufactured in substantially the same manner as in Comparative Example 1, except that Compound 2-3 was used instead of TPBi in forming an electron transport layer, and Compound 200-3 was used instead of mCP as a host.

Example 7

An organic light-emitting device was manufactured in substantially the same manner as in Comparative Example 1, except that Compound 2-5 was used instead of TPBi in forming an electron transport layer, and Compound 200-5 was used instead of mCP as a host.

The driving voltage, luminance, external quantum efficiency (EQE), and lifespan of the organic light-emitting devices manufactured according to Examples 1 to 7 and Comparative Examples 1 to 5 were manufactured, and results thereof are shown in Table 3.

TABLE 3 Electron transporting Driving Lifespan material Host voltage (V) EQE(%) T95 (hr) Comparative TPBi mCP 4.8 3.6 1 Example 1 Comparative 100 mCP 4.2 5.0 11 Example 2 Comparative 101 mCP 4.3 3.4 18 Example 3 Comparative 102 mCP 4.8 3.9 5 Example 4 Comparative 103 mCP 3.7 6.7 24 Example 5 Example 1 1-4 mCP 3.8 6.1 25 Example 2 2-3 mCP 3.3 9.4 51 Example 3 2-7 mCP 3.5 8.3 43 Example 4 6-1 mCP 3.9 5.6 13 Example 5  7-10 mCP 3.9 4.3 10 Example 6 2-3 200-3 3.2 10.2 87 Example 7 2-5 200-5 3.4 9.9 71

From Table 3, it can be seen that the organic light-emitting devices of Examples 1 to 7 exhibit excellent results, as compared with the organic light-emitting devices of Comparative Examples 1 to 5. This is consistent with that expected in the simulation results of Table 2.

The organic light-emitting device including the compound represented by Formula 1 may exhibit excellent efficiency and improved lifespan.

It should be understood that embodiments described herein should be considered in a descriptive sense only and not for purposes of limitation. Descriptions of features or aspects within each embodiment should be considered as available for other similar features or aspects in other embodiments.

While one or more embodiments have been described with reference to the figures, it will be understood by those of ordinary skill in the art that various changes in form and details may be made therein without departing from the spirit and scope of the present disclosure as defined by the following claims, and equivalents thereof. 

What is claimed is:
 1. A compound represented by Formula 1:

wherein, in Formula 1, A is a single bond linking X₃ with X₄, or A is a fused C₄-C₆₀ carbocyclic group or a fused C₁-C₆₀ heterocyclic group, X₁ is N, C, or C(R₁₁), X₂ is N, C, or C(R₁₂), X₃ is N, C, or C(R₁₃), X₄ is N, C, or C(R₁₄), X₅ is N, C, or C(R₁₅), and X₆ is N, C, or C(R₁₆), Y₁ is N or C(R₂₁), Y₂ is N or C(R₂₂), Y₃ is N or C(R₂₃), and at least one of Y₁ to Y₃ is N, R₁ to R₄, R₁₁ to R₁₆, and R₂₁ to R₂₃ are each independently selected from hydrogen, deuterium, a substituted or unsubstituted C₁-C₆₀ alkyl group, a substituted or unsubstituted C₂-C₆₀ alkenyl group, a substituted or unsubstituted C₂-C₆₀ alkynyl group, a substituted or unsubstituted C₁-C₆₀ alkoxy group, a substituted or unsubstituted C₃-C₁₀ cycloalkyl group, a substituted or unsubstituted C₁-C₁₀ heterocycloalkyl group, a substituted or unsubstituted C₃-C₁₀ cycloalkenyl group, a substituted or unsubstituted C₁-C₁₀ heterocycloalkenyl group, a substituted or unsubstituted C₆-C₆₀ aryl group, a substituted or unsubstituted C₆-C₆₀ aryloxy group, a substituted or unsubstituted C₆-C₆₀ arylthio group, a substituted or unsubstituted C₁-C₆₀ heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group, —Si(Q₁)(Q₂)(Q₃), —N(Q₁)(Q₂), —B(Q₁)(Q₂), —P(Q₁)(Q₂), —C(═O)(Q₁), —S(═O)₂(Q₁), and —P(═O)(Q₁)(Q₂), two neighboring substituents selected from R₁ to R₄, R₁₁ to R₁₆, and R₂₁ to R₂₃ are linked with each other to form a ring, wherein when A is a single bond linking X₃ with X₄, each of X₁, X₂, X₅, and X₆ is CH, and each of X₃ and X₄ is C, R₁ is selected from deuterium, a substituted or unsubstituted C₁-C₆₀ alkyl group, a substituted or unsubstituted C₂-C₆₀ alkenyl group, a substituted or unsubstituted C₂-C₆₀ alkynyl group, a substituted or unsubstituted C₁-C₆₀ alkoxy group, a substituted or unsubstituted C₃-C₁₀ cycloalkyl group, a substituted or unsubstituted C₁-C₁₀ heterocycloalkyl group, a substituted or unsubstituted C₃-C₁₀ cycloalkenyl group, a substituted or unsubstituted C₁-C₁₀ heterocycloalkenyl group, a substituted or unsubstituted C₆-C₆₀ aryl group, a substituted or unsubstituted C₆-C₆₀ aryloxy group, a substituted or unsubstituted C₆-C₆₀ arylthio group, a substituted or unsubstituted C₁-C₆₀ heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group, —Si(Q₁)(Q₂)(Q₃), —N(Q₁)(Q₂), —B(Q₁)(Q₂), —P(Q₁)(Q₂), —C(═O)(Q₁), —S(═O)₂(Q₁), and —P(═O)(Q₁)(Q₂), and at least one of Y₁ to Y₃ is C(R₂₁), C(R₂₂), or C(R₂₃), respectively, L is selected from a substituted or unsubstituted C₄-C₆₀ carbocyclic group and a substituted or unsubstituted C₁-C₆₀ heterocyclic group, when A is benzene, L or a moiety comprising Y₁ to Y₃ is linked with a carbon of position 3 (numerals 2 and 3 are carbon positions where L; or the moiety comprising Y₁ to Y₃ is linked to the moiety including A), m is an integer from 0 to 3, a is 1 or 2, b is an integer from 1 to 4, c and d are each independently an integer from 1 to 5, at least one substituent of the substituted C₁-C₆ alkyl group, the substituted C₂-C₆₀ alkenyl group, the substituted C₂-C₆₀ alkynyl group, the substituted C₁-C₆₀ alkoxy group, the substituted C₃-C₁₀ cycloalkyl group, the substituted C₁-C₁₀ heterocycloalkyl group, the substituted C₃-C₁₀ cycloalkenyl group, the substituted C₁-C₁₀ heterocycloalkenyl group, the substituted C₆-C₆₀ aryl group, the substituted C₆-C₆₀ arylene group, the substituted C₆-C₆₀ aryloxy group, the substituted C₆-C₆₀ arylthio group, the substituted C₁-C₆₀ heteroaryl group, the substituted C₁-C₆₀ heteroarylene group, the substituted monovalent non-aromatic condensed polycyclic group, the substituted monovalent non-aromatic condensed heteropolycyclic group, the substituted C₄-C₆₀ carbocyclic group, and the substituted C₁-C₆₀ heterocyclic group is selected from: deuterium (-D), —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, and a C₁-C₆₀ alkoxy group; a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, and a C₁-C₆₀ alkoxy group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, a monovalent non-aromatic condensed heteropolycyclic group, —Si(Q₁₁)(Q₁₂)(Q₁₃), —N(Q₁₁)(Q₁₂), —B(Q₁₁)(Q₁₂), —C(═O)(Q₁₁), —S(═O)₂(Q₁₁), and —P(═O)(Q₁₁)(Q₁₂); a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, and a monovalent non-aromatic condensed heteropolycyclic group; a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, and a monovalent non-aromatic condensed heteropolycyclic group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, a monovalent non-aromatic condensed heteropolycyclic group, —Si(Q₂₁)(Q₂₂)(Q₂₃), —N(Q₂₁)(Q₂₂), —B(Q₂₁)(Q₂₂), —C(═O)(Q₂₁), —S(═O)₂(Q₂₁), and —P(═O)(Q₂₁)(Q₂₂); and —Si(Q₃₁)(Q₃₂)(Q₃₃), —N(Q₃₁)(Q₃₂), —B(Q₃₁)(Q₃₂), —C(═O)(Q₃₁), —S(═O)₂(Q₃₁), and —P(═O)(Q₃₁)(Q₃₂), and Q₁ to Q₃, Q₁₁ to Q₁₃, Q₂₁ to Q₂₃, and Q₃₁ to Q₃₃ are each independently selected from hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a C₁-C₆ alkoxy group, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₁-C₆ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, a monovalent non-aromatic condensed heteropolycyclic group, a biphenyl group, and a terphenyl group.
 2. The compound of claim 1, wherein X₁ is C or C(R₁₁), X₂ is C or C(R₁₂), X₃ is C or C(R₁₃), X₄ is C or C(R₁₄), X₅ is C or C(R₁₅), and X₆ is C or C(R₁₆).
 3. The compound of claim 1, wherein X₂ is C or C(R₁₂), X₅ is C or C(R₁₅), and each of X₁ and X₆ is N.
 4. The compound of claim 1, wherein each of X₂ and X₅ is N, X₁ is C or C(R₁₁), and X₆ is C or C(R₁₆).
 5. The compound of claim 1, wherein A is a single bond linking X₃ with X₄, or indicates a fused cyclopentane, a fused benzene, a fused naphthalene, or a fused quinoxaline.
 6. The compound of claim 1, wherein each of R₂ to R₄ is hydrogen or deuterium.
 7. The compound of claim 1, wherein L is selected from a phenylene group, a naphthylene group, a phenanthrenylene group, an anthracenylene group, a pyrenylene group, a chrysenylene group, a pyridinylene group, a pyrazinylene group, a pyrimidinylene group, a pyridazinylene group, a quinolinylene group, an isoquinolinylene group, a quinoxalinylene group, a quinazolinylene group, a carbazolylene group, and a triazinylene group.
 8. The compound of claim 1, wherein Formula 1 is represented by one of Formulae 1-1 to 1-7:

wherein, in Formulae 1-1 to 1-4 and 1-7, R′₂ and R″₂ are each independently the same as defined in connection with R₂ in Formula 1, and in Formula 1-5, R₁ is selected from deuterium, a substituted or unsubstituted C₁-C₆₀ alkyl group, a substituted or unsubstituted C₂-C₆₀ alkenyl group, a substituted or unsubstituted C₂-C₆₀ alkynyl group, a substituted or unsubstituted C₁-C₆₀ alkoxy group, a substituted or unsubstituted C₃-C₁₀ cycloalkyl group, a substituted or unsubstituted C₁-C₁₀ heterocycloalkyl group, a substituted or unsubstituted C₃-C₁₀ cycloalkenyl group, a substituted or unsubstituted C₁-C₁₀ heterocycloalkenyl group, a substituted or unsubstituted C₆-C₆₀ aryl group, a substituted or unsubstituted C₆-C₆₀ aryloxy group, a substituted or unsubstituted C₆-C₆₀ arylthio group, a substituted or unsubstituted C₁-C₆₀ heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group, —Si(Q₁)(Q₂)(Q₃), —N(Q₁)(Q₂), —B(Q₁)(Q₂), —P(Q₁)(Q₂), —C(═O)(Q₁), —S(═O)₂(Q₁), and —P(═O)(Q₁)(Q₂).
 9. The compound of claim 1, wherein R₁ is selected from hydrogen, deuterium, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a phenanthrenyl group, an anthracenyl group, a pyrenyl group, a chrysenyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, a quinolinyl group, an isoquinolinyl group, a quinoxalinyl group, a quinazolinyl group, a carbazolyl group, a benzofuropyridyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a triazinyl group, a benzimidazolyl group, and a phenanthrolinyl group.
 10. The compound of claim 1, wherein R₁ is represented by hydrogen, deuterium, or a group represented by one of Formulae 2a and 2b:

wherein, in Formulae 2a and 2b, R₂₁ to R₂₃ are each independently selected from hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazino group, a hydrazono group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₂₀ alkyl group, a C₁-C₂₀ alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a phenanthrenyl group, an anthracenyl group, a pyrenyl group, a chrysenyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, a quinolinyl group, an isoquinolinyl group, a quinoxalinyl group, a quinazolinyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a triazinyl group, a benzimidazolyl group, and a phenanthrolinyl group, a21 is an integer from 1 to 4, a22 is 1 or 2, a23 is an integer from 1 to 3, and * indicates a binding site to a neighboring atom.
 11. The compound of claim 1, wherein the compound represented by Formula 1 is one of the following compounds:


12. An organic light-emitting device comprising: a first electrode; a second electrode facing the first electrode; and an organic layer between the first electrode and the second electrode and comprising an emission layer, wherein the organic layer comprises the compound of claim
 1. 13. The organic light-emitting device of claim 12, wherein the first electrode is an anode, the second electrode is a cathode, the organic layer between the first electrode and the second electrode and comprising the emission layer further comprises i) a hole transport region between the first electrode and the emission layer and comprising a hole injection layer, a hole transport layer, a buffer layer, an electron blocking layer, or any combination thereof and ii) an electron transport region between the emission layer and the second electrode and comprising a hole blocking layer, an electron transport layer, an electron injection layer, or any combination thereof.
 14. The organic light-emitting device of claim 13, wherein the electron transport region comprises the compound represented by Formula
 1. 15. The organic light-emitting device of claim 13, wherein the electron transport layer comprises the compound represented by Formula
 1. 16. The organic light-emitting device of claim 13, wherein the compound chelates a metal compound migrating from the cathode.
 17. The organic light-emitting device of claim 12, wherein, the emission layer comprises a host, and the host comprises a compound represented by Formula 2:

wherein, in Formula 2, Ar₁ and Ar₂ are each independently selected from a substituted or unsubstituted C₆-C₆₀ aryl group and a substituted or unsubstituted C₁-C₆ heteroaryl group, R₁ to R₇ are each independently selected from hydrogen, deuterium, a substituted or unsubstituted C₁-C₆₀ alkyl group, a substituted or unsubstituted C₆-C₆₀ aryl group, a substituted or unsubstituted C₁-C₆₀ heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, and a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group, at least one substituent of the substituted C₁-C₆ alkyl group, the substituted C₆-C₆₀ aryl group, the substituted C₁-C₆₀ heteroaryl group, the substituted monovalent non-aromatic condensed polycyclic group, and the substituted monovalent non-aromatic condensed heteropolycyclic group is selected from: deuterium (-D), —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, and a C₁-C₆₀ alkoxy group; a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, and a C₁-C₆₀ alkoxy group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, a monovalent non-aromatic condensed heteropolycyclic group, —Si(Q₁₁)(Q₁₂)(Q₁₃), —N(Q₁₁)(Q₁₂), —B(Q₁₁)(Q₁₂), —C(═O)(Q₁₁), —S(═O)₂(Q₁₁), and —P(═O)(Q₁₁)(Q₁₂); a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, and a monovalent non-aromatic condensed heteropolycyclic group; a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, and a monovalent non-aromatic condensed heteropolycyclic group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, a monovalent non-aromatic condensed heteropolycyclic group, —Si(Q₂₁)(Q₂₂)(Q₂₃), —N(Q₂₁)(Q₂₂), —B(Q₂₁)(Q₂₂), —C(═O)(Q₂₁), —S(═O)₂(Q₂₁), and —P(═O)(Q₂₁)(Q₂₂); and —Si(Q₃₁)(Q₃₂)(Q₃₃), —N(Q₃₁)(Q₃₂), —B(Q₃₁)(Q₃₂), —C(═O)(Q₃₁), —S(═O)₂(Q₃₁), and —P(═O)(Q₃₁)(Q₃₂), and Q₁ to Q₃, Q₁₁ to Q₁₃, Q₂₁ to Q₂₃, and Q₃₁ to Q₃₃ are each independently selected from hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a C₁-C₆ alkoxy group, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₁-C₆ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, a monovalent non-aromatic condensed heteropolycyclic group, a biphenyl group, and a terphenyl group.
 18. The organic light-emitting device of claim 17, wherein the compound represented by Formula 2 is selected from the following compounds:


19. The organic light-emitting device of claim 12, wherein the emission layer comprises quantum dots.
 20. An electronic apparatus comprising: a thin-film transistor; and the organic light-emitting device of claim 12, wherein the thin-film transistor comprises a source electrode, a drain electrode, an activation layer, and a gate electrode, and the first electrode of the organic light-emitting device is in electrical contact with one of the source electrode and the drain electrode of the thin-film transistor. 